Variant report

Variant	nsv1033347
Chromosome Location	chr4:144288438-144299563
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	ATF2	chr4:144297148-144297630	GM12878	blood:	n/a	n/a
2	ATF2	chr4:144298593-144299412	GM12878	blood:	n/a	n/a
3	ATF2	chr4:144298635-144299351	GM12878	blood:	n/a	n/a
4	ATF2	chr4:144293283-144294071	GM12878	blood:	n/a	n/a
5	ATF2	chr4:144293374-144294131	GM12878	blood:	n/a	n/a
6	BATF	chr4:144293442-144294070	GM12878	blood:	n/a	chr4:144293727-144293738
7	BATF	chr4:144297351-144297543	GM12878	blood:	n/a	n/a
8	BATF	chr4:144293469-144293997	GM12878	blood:	n/a	chr4:144293727-144293738
9	BCL11A	chr4:144293420-144294104	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:144293593-144293987	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:144298783-144299242	GM12878	blood:	n/a	chr4:144299002-144299011 chr4:144298844-144298853
12	BCL3	chr4:144293534-144294035	GM12878	blood:	n/a	n/a
13	BCL3	chr4:144298720-144299294	GM12878	blood:	n/a	chr4:144299002-144299011 chr4:144298844-144298853
14	BCLAF1	chr4:144298700-144299448	GM12878	blood:	n/a	chr4:144299002-144299011 chr4:144298844-144298853
15	BCLAF1	chr4:144293238-144294109	GM12878	blood:	n/a	n/a
16	BCLAF1	chr4:144293417-144294065	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:144293281-144294215	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:144298356-144299297	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:144295414-144295437	K562	blood:	n/a	n/a
20	CEBPB	chr4:144291986-144292321	A549	lung:	n/a	chr4:144292145-144292156
21	CEBPB	chr4:144291985-144292186	HepG2	liver:	n/a	chr4:144292145-144292156
22	CEBPB	chr4:144292998-144294244	GM12878	blood:	n/a	n/a
23	CEBPB	chr4:144291964-144292167	IMR90	lung:	n/a	chr4:144292145-144292156
24	CEBPB	chr4:144298704-144299319	GM12878	blood:	n/a	n/a
25	CEBPB	chr4:144291988-144292177	K562	blood:	n/a	chr4:144292145-144292156
26	CEBPD	chr4:144296427-144296920	K562	blood:	n/a	n/a
27	CEBPD	chr4:144296528-144296937	K562	blood:	n/a	n/a
28	CHD1	chr4:144293294-144294050	GM12878	blood:	n/a	n/a
29	CHD1	chr4:144297544-144297881	GM12878	blood:	n/a	n/a
30	CHD1	chr4:144298552-144299492	GM12878	blood:	n/a	n/a
31	CHD2	chr4:144298791-144299720	GM12878	blood:	n/a	n/a
32	CHD2	chr4:144293364-144294164	GM12878	blood:	n/a	n/a
33	CREB1	chr4:144298594-144299403	GM12878	blood:	n/a	n/a
34	CREB1	chr4:144293375-144294035	GM12878	blood:	n/a	n/a
35	CTCF	chr4:144296520-144296670	HEK293	kidney:	n/a	chr4:144296581-144296591 chr4:144296578-144296596 chr4:144296573-144296594 chr4:144296584-144296593 chr4:144296579-144296595
36	CTCF	chr4:144296960-144297110	A549	lung:	n/a	n/a
37	CTCF	chr4:144296540-144296690	HCFaa	heart:	n/a	chr4:144296581-144296591 chr4:144296578-144296596 chr4:144296573-144296594 chr4:144296584-144296593 chr4:144296579-144296595
38	CTCF	chr4:144296580-144296730	SAEC	small airway:	n/a	chr4:144296581-144296591 chr4:144296584-144296593
39	CTCF	chr4:144296520-144296670	GM12878	blood:	n/a	chr4:144296581-144296591 chr4:144296578-144296596 chr4:144296573-144296594 chr4:144296584-144296593 chr4:144296579-144296595
40	CTCF	chr4:144296900-144297050	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr4:144296940-144297090	GM12871	blood:	n/a	n/a
42	CTCF	chr4:144296794-144297217	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:144296499-144296733	MCF-7	breast:	n/a	chr4:144296581-144296591 chr4:144296578-144296596 chr4:144296573-144296594 chr4:144296584-144296593 chr4:144296579-144296595
44	CTCF	chr4:144296880-144297030	AG09309	skin:	n/a	n/a
45	CTCF	chr4:144296920-144297070	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr4:144296813-144297079	A549	lung:	n/a	n/a
47	CTCF	chr4:144296860-144297010	RPTEC	kidney:	n/a	n/a
48	CTCF	chr4:144296880-144297030	HRE	kidney:	n/a	n/a
49	CTCF	chr4:144296540-144296690	GM12868	blood:	n/a	chr4:144296581-144296591 chr4:144296578-144296596 chr4:144296573-144296594 chr4:144296584-144296593 chr4:144296579-144296595
50	CTCF	chr4:144296940-144297090	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:144297236-144297286	Caco-2	colon:	n/a
2	chr4:144297236-144297286	SKMC	muscle:	n/a
3	chr4:144297236-144297286	HUVEC	blood vessel:	n/a
4	chr4:144297236-144297286	HCM	heart:	n/a
5	chr4:144297236-144297286	SK-N-SH_RA	brain:	n/a
6	chr4:144297236-144297286	Hepatocyte	liver:	n/a
7	chr4:144297236-144297286	NHBE	bronchial:	n/a
8	chr4:144297236-144297286	HRPEpiC	eye:	n/a
9	chr4:144297236-144297286	HIPEpiC	eye:	n/a
10	chr4:144297236-144297286	IMR90	lung:	fetal
11	chr4:144297236-144297286	GM12891	blood:	n/a
12	chr4:144297236-144297286	AG09319	gingival:	n/a
13	chr4:144297236-144297286	SK-N-MC	brain:	n/a
14	chr4:144297236-144297286	SAEC	small airway:	n/a
15	chr4:144297236-144297286	PrEC	prostate:	n/a
16	chr4:144297236-144297286	BE2_C	brain:	n/a
17	chr4:144297236-144297286	HMEC	breast:	n/a
18	chr4:144297236-144297286	GM19239	blood:	n/a
19	chr4:144297236-144297286	AG04449	skin:	fetal
20	chr4:144297236-144297286	AG04450	lung:	fetal
21	chr4:144297236-144297286	AG10803	skin:	n/a
22	chr4:144297236-144297286	HepG2	liver:	n/a
23	chr4:144297236-144297286	HL-60	blood:	n/a
24	chr4:144297236-144297286	Jurkat	blood:	n/a
25	chr4:144297236-144297286	AoSMC	blood vessel:	n/a
26	chr4:144297236-144297286	HRCEpiC	kidney:	n/a
27	chr4:144297236-144297286	ProgFib	skin:	n/a
28	chr4:144297236-144297286	K562	blood:	n/a
29	chr4:144297236-144297286	HCPEpiC	choroid plexus:	n/a
30	chr4:144297236-144297286	U87	brain:	n/a
31	chr4:144297236-144297286	HEK293	kidney:	embryo
32	chr4:144297236-144297286	GM12878	blood:	n/a
33	chr4:144297236-144297286	HCF	heart:	n/a
34	chr4:144297236-144297286	T-47D	breast:	n/a
35	chr4:144297236-144297286	LNCaP	prostate:	n/a
36	chr4:144297236-144297286	H1-hESC	embryonic stem cell:	embryo
37	chr4:144297236-144297286	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:144297236-144297286	BJ	skin:	n/a
39	chr4:144297236-144297286	GM12892	blood:	n/a
40	chr4:144297236-144297286	Hela-S3	cervix:	n/a
41	chr4:144297236-144297286	MCF-7	breast:	n/a
42	chr4:144297236-144297286	ECC-1	luminal epithelium:	n/a
43	chr4:144297236-144297286	A549	lung:	n/a
44	chr4:144297236-144297286	PANC-1	pancreas:	n/a
45	chr4:144297236-144297286	HRE	kidney:	n/a
46	chr4:144297236-144297286	AG09309	skin:	n/a
47	chr4:144297236-144297286	ovcar-3	ovarian:	n/a
48	chr4:144297236-144297286	HCT-116	colon:	n/a
49	chr4:144297236-144297286	HAEpiC	amniotic membrane:	n/a
50	chr4:144297236-144297286	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:144295435..144296093-chr5:75459165..75460000,2	MCF-7	breast:
2	chr4:144294005..144295749-chr4:144303829..144305469,2	K562	blood:
3	chr4:144296798..144297742-chr4:144403694..144404468,2	MCF-7	breast:
4	chr4:144284857..144287398-chr4:144288484..144291385,2	K562	blood:
5	chr4:144289833..144292177-chr4:144294492..144296058,2	K562	blood:
6	chr4:144290996..144292995-chr4:144295055..144297084,2	MCF-7	breast:
7	chr4:144256664..144258280-chr4:144293930..144296084,2	MCF-7	breast:
8	chr4:144289833..144292177-chr4:144294492..144296058,2	K562	blood:
9	chr4:144289833..144291469-chr4:144294402..144296058,2	K562	blood:
10	chr4:144257935..144259880-chr4:144296110..144298167,2	MCF-7	breast:
11	chr4:144292852..144297100-chr4:144298409..144302941,5	K562	blood:
12	chr4:144283863..144286903-chr4:144287176..144291126,4	K562	blood:
13	chr4:144292852..144297100-chr4:144298409..144302941,5	K562	blood:
14	chr4:144279254..144282177-chr4:144295139..144296728,2	MCF-7	breast:
15	chr4:144290996..144292995-chr4:144295055..144297084,2	MCF-7	breast:
16	chr4:144254627..144258395-chr4:144297952..144301828,4	K562	blood:
17	chr4:144296980..144297503-chr4:144403654..144404586,2	MCF-7	breast:
18	chr4:144289833..144291469-chr4:144294402..144296058,2	K562	blood:
19	chr4:144299400..144301389-chr4:144302183..144304339,2	K562	blood:

Variant related genes	Relation type
GAB1	TF binding region
GAB1	CpG island
ENSG00000178972	chromatin interactions
ENSG00000109458	chromatin interactions

Extended variants
information (count: 391 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141034023	chr4:144288446-144288447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs57336725	chr4:144288494-144288495	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs572134378	chr4:144288537-144288538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs28684892	chr4:144288551-144288552	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs145089518	chr4:144288577-144288578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs56352863	chr4:144288599-144288600	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs564931881	chr4:144288603-144288604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577003066	chr4:144288611-144288612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs2055730	chr4:144288653-144288654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs55683567	chr4:144288675-144288676	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs529708708	chr4:144288677-144288678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549384285	chr4:144288693-144288694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs33926534	chr4:144288706-144288707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572623206	chr4:144288707-144288708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554124046	chr4:144288719-144288720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200401530	chr4:144288720-144288721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74973720	chr4:144288731-144288732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531774980	chr4:144288737-144288738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549955804	chr4:144288744-144288745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571553762	chr4:144288747-144288748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532445818	chr4:144288756-144288757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547516899	chr4:144288758-144288759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371349213	chr4:144288773-144288774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181169139	chr4:144288801-144288802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199879990	chr4:144288871-144288872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs71588248	chr4:144288872-144288873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574025621	chr4:144288878-144288879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565898570	chr4:144289028-144289029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536671522	chr4:144289037-144289038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540004078	chr4:144289058-144289059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554520736	chr4:144289078-144289079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564949439	chr4:144289158-144289159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs77815966	chr4:144289246-144289247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs1472873	chr4:144289305-144289306	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs577145181	chr4:144289336-144289337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541094075	chr4:144289369-144289370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544164680	chr4:144289384-144289385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553126317	chr4:144289390-144289391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs3805253	chr4:144289502-144289503	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs541821145	chr4:144289579-144289580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563178390	chr4:144289598-144289599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377273486	chr4:144289610-144289611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs300909	chr4:144289616-144289617	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs140696819	chr4:144289673-144289674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6820333	chr4:144289717-144289718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548492658	chr4:144289720-144289721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185384028	chr4:144289733-144289734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368599046	chr4:144289748-144289749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189699356	chr4:144289749-144289750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs80146199	chr4:144289774-144289775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22048815	CNVD
Autism	22241247	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:451 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:144272800-144299800	Weak transcription	Fetal Muscle Trunk	muscle
2	chr4:144277200-144290400	Weak transcription	Pancreas	Pancrea
3	chr4:144277400-144296800	Weak transcription	HSMMtube	muscle
4	chr4:144281200-144290000	Weak transcription	Fetal Stomach	stomach
5	chr4:144281200-144296800	Weak transcription	Fetal Muscle Leg	muscle
6	chr4:144281400-144296800	Weak transcription	Fetal Kidney	kidney
7	chr4:144281800-144293400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:144282000-144291200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr4:144282800-144290600	Weak transcription	Fetal Lung	lung
10	chr4:144283000-144290600	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr4:144283000-144290800	Weak transcription	Primary B cells from cord blood	blood
12	chr4:144283000-144290800	Weak transcription	Gastric	stomach
13	chr4:144283000-144291200	Weak transcription	Ovary	ovary
14	chr4:144283000-144293400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr4:144283000-144295400	Weak transcription	Stomach Smooth Muscle	stomach
16	chr4:144283000-144302200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr4:144283200-144293400	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr4:144284000-144293600	Weak transcription	Spleen	Spleen
19	chr4:144284000-144296600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr4:144284000-144296600	Weak transcription	Fetal Thymus	thymus
21	chr4:144284200-144295600	Weak transcription	Duodenum Mucosa	Duodenum
22	chr4:144284400-144290600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr4:144284400-144299400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:144284600-144290000	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr4:144284600-144290000	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr4:144284600-144290800	Weak transcription	Fetal Intestine Large	intestine
27	chr4:144284600-144291200	Weak transcription	Fetal Intestine Small	intestine
28	chr4:144284600-144295200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr4:144284600-144295200	Weak transcription	K562	blood
30	chr4:144284800-144290000	Weak transcription	Brain Angular Gyrus	brain
31	chr4:144284800-144295600	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr4:144285000-144290000	Weak transcription	Small Intestine	intestine
33	chr4:144285000-144290400	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr4:144285000-144290800	Weak transcription	Right Ventricle	heart
35	chr4:144285200-144290000	Weak transcription	Left Ventricle	heart
36	chr4:144285200-144290000	Weak transcription	Lung	lung
37	chr4:144285200-144290000	Weak transcription	Psoas Muscle	Psoas
38	chr4:144285200-144290000	Weak transcription	Right Atrium	heart
39	chr4:144285200-144290600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr4:144285400-144290000	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr4:144286000-144290600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr4:144286000-144291200	Weak transcription	Aorta	Aorta
43	chr4:144286000-144293400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr4:144286000-144294600	Weak transcription	Placenta	Placenta
45	chr4:144286000-144295800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr4:144286000-144298200	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr4:144287200-144290800	Weak transcription	Fetal Heart	heart
48	chr4:144287400-144290600	Weak transcription	Brain Anterior Caudate	brain
49	chr4:144287400-144294400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr4:144288200-144290000	Weak transcription	Brain Substantia Nigra	brain

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