Variant report

Variant	nsv877538
Chromosome Location	chr3:138218709-138311201
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:288)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:138232341-138232746	GM12878	blood:	n/a	n/a
2	BATF	chr3:138232282-138232701	GM12878	blood:	n/a	n/a
3	BATF	chr3:138232250-138232641	GM12878	blood:	n/a	n/a
4	BATF	chr3:138290753-138291213	GM12878	blood:	n/a	n/a
5	BATF	chr3:138290836-138291217	GM12878	blood:	n/a	n/a
6	BCL11A	chr3:138232380-138232593	GM12878	blood:	n/a	n/a
7	BCL11A	chr3:138232300-138232602	GM12878	blood:	n/a	n/a
8	BCL3	chr3:138307165-138307494	GM12878	blood:	n/a	n/a
9	BCLAF1	chr3:138232232-138232651	GM12878	blood:	n/a	n/a
10	BRCA1	chr3:138226822-138227373	Hela-S3	cervix:	n/a	chr3:138226971-138226978
11	CBX3	chr3:138264471-138264803	K562	blood:	n/a	n/a
12	CBX3	chr3:138264516-138264738	K562	blood:	n/a	n/a
13	CEBPB	chr3:138288564-138288798	MCF-7	breast:	n/a	chr3:138288660-138288671
14	CEBPB	chr3:138228476-138228768	IMR90	lung:	n/a	n/a
15	CEBPB	chr3:138281801-138282056	HepG2	liver:	n/a	chr3:138281950-138281961
16	CEBPB	chr3:138288628-138288758	K562	blood:	n/a	chr3:138288660-138288671
17	CEBPB	chr3:138288613-138288832	Hela-S3	cervix:	n/a	chr3:138288660-138288671
18	CEBPB	chr3:138288565-138288831	HepG2	liver:	n/a	chr3:138288660-138288671
19	CEBPB	chr3:138252220-138252307	K562	blood:	n/a	chr3:138252226-138252237 chr3:138252224-138252237 chr3:138252224-138252237
20	CEBPB	chr3:138270609-138270801	HepG2	liver:	n/a	chr3:138270721-138270732
21	CEBPB	chr3:138270604-138270843	IMR90	lung:	n/a	chr3:138270721-138270732
22	CEBPB	chr3:138288558-138288802	IMR90	lung:	n/a	chr3:138288660-138288671
23	CEBPB	chr3:138221907-138222107	HepG2	liver:	n/a	n/a
24	CEBPB	chr3:138270675-138270800	A549	lung:	n/a	chr3:138270721-138270732
25	CHD1	chr3:138297122-138297309	GM12878	blood:	n/a	n/a
26	CHD2	chr3:138297131-138297320	GM12878	blood:	n/a	n/a
27	CTCF	chr3:138286280-138286430	GM12867	blood:	n/a	n/a
28	CTCF	chr3:138286329-138286466	HepG2	liver:	n/a	n/a
29	CTCF	chr3:138286340-138286502	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr3:138286280-138286430	GM06990	blood:	n/a	n/a
31	CTCF	chr3:138286307-138286531	MCF-7	breast:	n/a	n/a
32	CTCF	chr3:138286325-138286493	LNCaP	prostate:	n/a	n/a
33	CTCF	chr3:138257928-138258007	LNCaP	prostate:	n/a	n/a
34	CTCF	chr3:138286240-138286390	NHEK	skin:	n/a	n/a
35	CTCF	chr3:138286300-138286450	GM12878	blood:	n/a	n/a
36	CTCF	chr3:138285880-138286030	Caco-2	colon:	n/a	n/a
37	CTCF	chr3:138286345-138286467	GM12878	blood:	n/a	n/a
38	CTCF	chr3:138286320-138286470	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr3:138286261-138286523	K562	blood:	n/a	n/a
40	CTCF	chr3:138286400-138286550	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr3:138286165-138286536	MCF-7	breast:	n/a	n/a
42	CTCF	chr3:138286360-138286510	GM12871	blood:	n/a	n/a
43	CTCF	chr3:138286180-138286330	RPTEC	kidney:	n/a	n/a
44	CTCF	chr3:138286260-138286410	GM12872	blood:	n/a	n/a
45	CTCF	chr3:138286340-138286490	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr3:138286320-138286470	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:138286340-138286490	MCF-7	breast:	n/a	n/a
48	CTCF	chr3:138286260-138286410	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr3:138286380-138286530	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr3:138259280-138259362	GM10248	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:138309376-138309426	SK-N-MC	brain:	n/a
2	chr3:138231780-138231830	LNCaP	prostate:	n/a
3	chr3:138309376-138309426	MCF-7	breast:	n/a
4	chr3:138231780-138231830	GM19239	blood:	n/a
5	chr3:138309376-138309426	BE2_C	brain:	n/a
6	chr3:138309376-138309426	HAEpiC	amniotic membrane:	n/a
7	chr3:138231780-138231830	HCT-116	colon:	n/a
8	chr3:138231780-138231830	PFSK-1	brain:	n/a
9	chr3:138231780-138231830	AG04449	skin:	fetal
10	chr3:138231780-138231830	NT2-D1	testis:	n/a
11	chr3:138309376-138309426	T-47D	breast:	n/a
12	chr3:138231780-138231830	NHDF-neo	bronchial:	n/a
13	chr3:138231780-138231830	PrEC	prostate:	n/a
14	chr3:138231780-138231830	NHBE	bronchial:	n/a
15	chr3:138231780-138231830	RPTEC	kidney:	n/a
16	chr3:138309376-138309426	Caco-2	colon:	n/a
17	chr3:138231780-138231830	BE2_C	brain:	n/a
18	chr3:138231780-138231830	ECC-1	luminal epithelium:	n/a
19	chr3:138231780-138231830	T-47D	breast:	n/a
20	chr3:138231780-138231830	GM12892	blood:	n/a
21	chr3:138231780-138231830	GM06990	blood:	n/a
22	chr3:138231780-138231830	MCF-7	breast:	n/a
23	chr3:138309376-138309426	HRE	kidney:	n/a
24	chr3:138231780-138231830	PANC-1	pancreas:	n/a
25	chr3:138309376-138309426	HRCEpiC	kidney:	n/a
26	chr3:138309376-138309426	HCT-116	colon:	n/a
27	chr3:138309376-138309426	ECC-1	luminal epithelium:	n/a
28	chr3:138309376-138309426	HNPCEpiC	eye:	n/a
29	chr3:138231780-138231830	ovcar-3	ovarian:	n/a
30	chr3:138231780-138231830	AG09319	gingival:	n/a
31	chr3:138309376-138309426	K562	blood:	n/a
32	chr3:138309376-138309426	PrEC	prostate:	n/a
33	chr3:138309376-138309426	AoSMC	blood vessel:	n/a
34	chr3:138309376-138309426	HL-60	blood:	n/a
35	chr3:138309376-138309426	AG09309	skin:	n/a
36	chr3:138231780-138231830	U87	brain:	n/a
37	chr3:138309376-138309426	U87	brain:	n/a
38	chr3:138309376-138309426	IMR90	lung:	fetal
39	chr3:138309376-138309426	H1-hESC	embryonic stem cell:	embryo
40	chr3:138231780-138231830	HRCEpiC	kidney:	n/a
41	chr3:138231780-138231830	SK-N-SH_RA	brain:	n/a
42	chr3:138309376-138309426	PFSK-1	brain:	n/a
43	chr3:138309376-138309426	ovcar-3	ovarian:	n/a
44	chr3:138231780-138231830	Caco-2	colon:	n/a
45	chr3:138309376-138309426	GM12878	blood:	n/a
46	chr3:138231780-138231830	Jurkat	blood:	n/a
47	chr3:138309376-138309426	GM12892	blood:	n/a
48	chr3:138231780-138231830	HMEC	breast:	n/a
49	chr3:138231780-138231830	IMR90	lung:	fetal
50	chr3:138231780-138231830	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr3:138308688..138311077-chr3:138311353..138314105,2	MCF-7	breast:
2	chr3:138222687..138224341-chr3:138230011..138232185,2	MCF-7	breast:
3	chr3:138285865..138286691-chr3:138634339..138635162,2	MCF-7	breast:
4	chr3:138306522..138308483-chr3:138311202..138313507,2	MCF-7	breast:
5	chr3:138228056..138229897-chr3:138230355..138233975,3	K562	blood:
6	chr3:138307055..138308900-chr3:138311564..138313452,3	K562	blood:
7	chr3:138309173..138314814-chr3:138323140..138328328,8	K562	blood:
8	chr3:138306109..138310037-chr3:138310110..138314269,4	MCF-7	breast:
9	chr3:138228056..138229897-chr3:138230355..138233975,3	K562	blood:
10	chr3:138305622..138307712-chr3:138326146..138327736,2	K562	blood:
11	chr2:197162739..197163660-chr3:138306734..138307658,2	MCF-7	breast:
12	chr3:138308891..138310571-chr3:138313902..138316460,2	K562	blood:
13	chr3:138309156..138310798-chr3:138631884..138634871,2	MCF-7	breast:
14	chr20:3451237..3451899-chr3:138226141..138226668,2	MCF-7	breast:
15	chr3:138291466..138294081-chr3:138311931..138314482,2	MCF-7	breast:
16	chr3:138222687..138224341-chr3:138230011..138232185,2	MCF-7	breast:
17	chr3:138310855..138313031-chr3:138326538..138329064,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIK3CB-1	chr3:138310708-138310798	NONHSAT092334

No data

Variant related genes	Relation type
CEP70	TF binding region
CEP70	CpG island
ENSG00000114107	chromatin interactions
ENSG00000158234	chromatin interactions
ENSG00000088812	chromatin interactions

Extended variants
information (count: 3652 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:3652 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7653815	chr3:138218709-138218710	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553976247	chr3:138218814-138218815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574177234	chr3:138218823-138218824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147084266	chr3:138218918-138218919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375807847	chr3:138218954-138218955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200730069	chr3:138218956-138218957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563049064	chr3:138218970-138218971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550727472	chr3:138218981-138218982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531685434	chr3:138218982-138218983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35340237	chr3:138218994-138218995	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs377499427	chr3:138219042-138219043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140569326	chr3:138219048-138219049	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368916780	chr3:138219056-138219057	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144294583	chr3:138219066-138219067	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565361288	chr3:138219210-138219211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373085659	chr3:138219230-138219231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs114744558	chr3:138219252-138219253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141208365	chr3:138219289-138219290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370409745	chr3:138219305-138219306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182373450	chr3:138219315-138219316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150201771	chr3:138219343-138219344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138631490	chr3:138219346-138219347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148908930	chr3:138219353-138219354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113169450	chr3:138219391-138219392	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553898863	chr3:138219409-138219410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs150622817	chr3:138219436-138219437	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111605907	chr3:138219437-138219438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371594314	chr3:138219460-138219461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11920599	chr3:138219517-138219518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538617017	chr3:138219518-138219519	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567096762	chr3:138219541-138219542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138506086	chr3:138219557-138219558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113264564	chr3:138219567-138219568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534389214	chr3:138219571-138219572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377207926	chr3:138219576-138219577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370054530	chr3:138219608-138219609	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200412030	chr3:138219614-138219615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138124965	chr3:138219618-138219619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376931648	chr3:138219632-138219633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143913326	chr3:138219649-138219650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556813754	chr3:138219664-138219665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576698082	chr3:138219669-138219670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34053101	chr3:138219674-138219675	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201668440	chr3:138219754-138219755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11920691	chr3:138219800-138219801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527701150	chr3:138219823-138219824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541494046	chr3:138219853-138219854	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561226496	chr3:138219874-138219875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs202216015	chr3:138219885-138219886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529893769	chr3:138219892-138219893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	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
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	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
Developmental delay	21147756	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138194000-138260200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr3:138207000-138223800	Weak transcription	Brain Anterior Caudate	brain
3	chr3:138208400-138227400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr3:138209400-138236800	Weak transcription	Aorta	Aorta
5	chr3:138209800-138258600	Weak transcription	Primary T cells from cord blood	blood
6	chr3:138210000-138230200	Weak transcription	Fetal Brain Male	brain
7	chr3:138210200-138222000	Weak transcription	Brain Hippocampus Middle	brain
8	chr3:138210400-138236800	Weak transcription	Brain Substantia Nigra	brain
9	chr3:138210400-138242000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr3:138210800-138260600	Weak transcription	Colonic Mucosa	Colon
11	chr3:138211000-138229400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:138211000-138231000	Weak transcription	Rectal Smooth Muscle	rectum
13	chr3:138211000-138236600	Weak transcription	Spleen	Spleen
14	chr3:138211200-138227200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr3:138211200-138260600	Weak transcription	Brain Angular Gyrus	brain
16	chr3:138211400-138230400	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr3:138211600-138227400	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr3:138211800-138260600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr3:138212000-138235000	Weak transcription	Brain Germinal Matrix	brain
20	chr3:138212000-138235800	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr3:138212400-138221200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr3:138212400-138236600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr3:138212400-138236600	Weak transcription	Esophagus	oesophagus
24	chr3:138212600-138224400	Weak transcription	Left Ventricle	heart
25	chr3:138212600-138236600	Weak transcription	Lung	lung
26	chr3:138212600-138250200	Weak transcription	Brain Cingulate Gyrus	brain
27	chr3:138212800-138236800	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr3:138212800-138249800	Weak transcription	Small Intestine	intestine
29	chr3:138213000-138224400	Weak transcription	Fetal Muscle Trunk	muscle
30	chr3:138213200-138236600	Weak transcription	Ovary	ovary
31	chr3:138213200-138236600	Weak transcription	Stomach Smooth Muscle	stomach
32	chr3:138213200-138243800	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr3:138213400-138230200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr3:138213600-138219600	Weak transcription	A549	lung
35	chr3:138213800-138220600	Weak transcription	Hela-S3	cervix
36	chr3:138213800-138231200	Weak transcription	Colon Smooth Muscle	Colon
37	chr3:138214200-138229000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr3:138214200-138229200	Weak transcription	Osteobl	bone
39	chr3:138214200-138232600	Weak transcription	HMEC	breast
40	chr3:138214200-138236600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr3:138214400-138220400	Weak transcription	NHLF	lung
42	chr3:138214400-138228600	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr3:138214400-138231800	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr3:138214400-138260600	Weak transcription	Right Ventricle	heart
45	chr3:138215000-138231800	Weak transcription	Psoas Muscle	Psoas
46	chr3:138215200-138223600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr3:138215400-138228800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr3:138215600-138226200	Weak transcription	Fetal Heart	heart
49	chr3:138215600-138236400	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr3:138215800-138218800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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