Variant report

Variant	nsv1024596
Chromosome Location	chr4:148830472-148886915
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:507)
CpG islands
(count:306)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:507 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:148864139-148864803	GM12878	blood:	n/a	chr4:148864728-148864735
2	ATF2	chr4:148864088-148864910	GM12878	blood:	n/a	chr4:148864728-148864735
3	BACH1	chr4:148871841-148872264	K562	blood:	n/a	n/a
4	BACH1	chr4:148872002-148872363	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr4:148864246-148864664	GM12878	blood:	n/a	n/a
6	BATF	chr4:148864272-148864651	GM12878	blood:	n/a	n/a
7	BCL11A	chr4:148864208-148864680	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:148864303-148864562	GM12878	blood:	n/a	n/a
9	BCLAF1	chr4:148864138-148864663	GM12878	blood:	n/a	n/a
10	BHLHE40	chr4:148878653-148878950	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:148865713-148865743	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:148864181-148864947	GM12878	blood:	n/a	n/a
13	CCNT2	chr4:148843357-148843586	K562	blood:	n/a	chr4:148843482-148843502
14	CEBPB	chr4:148886187-148886532	MCF-7	breast:	n/a	n/a
15	CEBPB	chr4:148885736-148886004	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:148862724-148862920	A549	lung:	n/a	n/a
17	CEBPB	chr4:148862663-148862930	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:148841496-148841564	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr4:148864660-148864810	A549	lung:	n/a	n/a
20	CEBPD	chr4:148843251-148843560	K562	blood:	n/a	n/a
21	CEBPD	chr4:148843282-148843583	K562	blood:	n/a	n/a
22	CHD2	chr4:148864288-148864770	GM12878	blood:	n/a	n/a
23	CREB1	chr4:148865257-148865888	GM12878	blood:	n/a	n/a
24	CREB1	chr4:148865401-148865749	GM12878	blood:	n/a	n/a
25	CREB1	chr4:148864192-148864940	GM12878	blood:	n/a	n/a
26	CREB1	chr4:148864155-148864725	GM12878	blood:	n/a	n/a
27	CTCF	chr4:148854637-148854805	HepG2	liver:	n/a	n/a
28	CTCF	chr4:148846300-148846450	HCT-116	colon:	n/a	n/a
29	CTCF	chr4:148854670-148854758	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr4:148846380-148846530	Caco-2	colon:	n/a	n/a
31	CTCF	chr4:148846309-148846596	MCF-7	breast:	n/a	n/a
32	CTCF	chr4:148848980-148849130	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr4:148854620-148854770	BJ	skin:	n/a	n/a
34	CTCF	chr4:148846360-148846510	WI-38	lung:	n/a	n/a
35	CTCF	chr4:148846380-148846530	GM12875	blood:	n/a	n/a
36	CTCF	chr4:148854640-148854790	GM12869	blood:	n/a	n/a
37	CTCF	chr4:148846380-148846530	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr4:148854680-148854791	MCF-7	breast:	n/a	n/a
39	CTCF	chr4:148854640-148854790	SAEC	small airway:	n/a	n/a
40	CTCF	chr4:148846360-148846510	HepG2	liver:	n/a	n/a
41	CTCF	chr4:148846340-148846490	NHEK	skin:	n/a	n/a
42	CTCF	chr4:148846380-148846530	HepG2	liver:	n/a	n/a
43	CTCF	chr4:148854600-148854750	GM12878	blood:	n/a	n/a
44	CTCF	chr4:148854660-148854810	GM12868	blood:	n/a	n/a
45	CTCF	chr4:148846393-148846506	GM10266	blood:	n/a	n/a
46	CTCF	chr4:148854576-148854808	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr4:148854643-148854774	GM13977	blood:	n/a	n/a
48	CTCF	chr4:148854653-148854804	K562	blood:	n/a	n/a
49	CTCF	chr4:148846380-148846530	AG04450	lung:	n/a	n/a
50	CTCF	chr4:148846340-148846575	A549	lung:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:148863880-148863930	IMR90	lung:	fetal
2	chr4:148863880-148863930	IMR90	lung:	fetal
3	chr4:148878178-148878228	AG04450	lung:	fetal
4	chr4:148885518-148885568	AG04449	skin:	fetal
5	chr4:148878178-148878228	HRCEpiC	kidney:	n/a
6	chr4:148861409-148861459	AG09319	gingival:	n/a
7	chr4:148848918-148848968	HRPEpiC	eye:	n/a
8	chr4:148863880-148863930	CMK	blood:	n/a
9	chr4:148878178-148878228	SK-N-SH	brain:	n/a
10	chr4:148885518-148885568	K562	blood:	n/a
11	chr4:148878178-148878228	AoSMC	blood vessel:	n/a
12	chr4:148885518-148885568	GM12892	blood:	n/a
13	chr4:148863880-148863930	ECC-1	luminal epithelium:	n/a
14	chr4:148848918-148848968	GM12892	blood:	n/a
15	chr4:148848918-148848968	MCF10A-Er-Src	breast:	n/a
16	chr4:148848918-148848968	PFSK-1	brain:	n/a
17	chr4:148861409-148861459	HCM	heart:	n/a
18	chr4:148878178-148878228	ovcar-3	ovarian:	n/a
19	chr4:148861409-148861459	U87	brain:	n/a
20	chr4:148885518-148885568	SK-N-SH_RA	brain:	n/a
21	chr4:148861409-148861459	Caco-2	colon:	n/a
22	chr4:148885518-148885568	HNPCEpiC	eye:	n/a
23	chr4:148863880-148863930	GM19239	blood:	n/a
24	chr4:148885518-148885568	HCM	heart:	n/a
25	chr4:148863880-148863930	BE2_C	brain:	n/a
26	chr4:148861409-148861459	IMR90	lung:	fetal
27	chr4:148863880-148863930	Jurkat	blood:	n/a
28	chr4:148863880-148863930	Hepatocyte	liver:	n/a
29	chr4:148848918-148848968	ECC-1	luminal epithelium:	n/a
30	chr4:148863880-148863930	HCF	heart:	n/a
31	chr4:148863880-148863930	HepG2	liver:	n/a
32	chr4:148878178-148878228	CMK	blood:	n/a
33	chr4:148885518-148885568	LNCaP	prostate:	n/a
34	chr4:148848918-148848968	HMEC	breast:	n/a
35	chr4:148848918-148848968	CMK	blood:	n/a
36	chr4:148861409-148861459	HEEpiC	esophagus:	n/a
37	chr4:148848918-148848968	HAEpiC	amniotic membrane:	n/a
38	chr4:148861409-148861459	CMK	blood:	n/a
39	chr4:148878178-148878228	BE2_C	brain:	n/a
40	chr4:148878178-148878228	ProgFib	skin:	n/a
41	chr4:148861409-148861459	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:148863880-148863930	HRPEpiC	eye:	n/a
43	chr4:148885518-148885568	HEEpiC	esophagus:	n/a
44	chr4:148878178-148878228	HEK293	kidney:	embryo
45	chr4:148848918-148848968	NHDF-neo	bronchial:	n/a
46	chr4:148863880-148863930	A549	lung:	n/a
47	chr4:148861409-148861459	NHDF-neo	bronchial:	n/a
48	chr4:148878178-148878228	SAEC	small airway:	n/a
49	chr4:148878178-148878228	GM12891	blood:	n/a
50	chr4:148878178-148878228	NT2-D1	testis:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:148846022..148846608-chr4:149073964..149074698,2	MCF-7	breast:
2	chr4:148447258..148447941-chr4:148845761..148846516,2	MCF-7	breast:
3	chr4:148846033..148846771-chr4:148975122..148975757,2	MCF-7	breast:
4	chr4:148870240..148873199-chr4:148874453..148876510,2	MCF-7	breast:
5	chr4:148870240..148873199-chr4:148874453..148876510,2	MCF-7	breast:
6	chr4:148881694..148883564-chr4:148895633..148897317,2	MCF-7	breast:
7	chr4:148851806..148854793-chr4:148858894..148861508,2	MCF-7	breast:
8	chr4:148844312..148847259-chr4:149048458..149051451,2	MCF-7	breast:
9	chr4:148603821..148605355-chr4:148862724..148865467,2	MCF-7	breast:
10	chr4:148851806..148854793-chr4:148858894..148861508,2	MCF-7	breast:
11	chr15:60771041..60771603-chr4:148849105..148849605,2	Hela-S3	cervix:
12	chr4:148884380..148886490-chr4:148890987..148892658,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NR3C2-5	chr4:148837680-148838537	NONHSAT098692

No data

Variant related genes	Relation type
ARHGAP10	TF binding region
ENSG00000270387	TF binding region
ARHGAP10	CpG island
ENSG00000270387	CpG island
ENSG00000245534	chromatin interactions
ENSG00000128915	chromatin interactions
ENSG00000164169	chromatin interactions

Extended variants
information (count: 2163 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2163 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1529935	chr4:148830472-148830473	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142149435	chr4:148830507-148830508	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs114239565	chr4:148830517-148830518	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs58443426	chr4:148830538-148830539	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs558646325	chr4:148830549-148830550	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs180753889	chr4:148830579-148830580	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541144495	chr4:148830649-148830650	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145907402	chr4:148830659-148830660	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369953865	chr4:148830674-148830675	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183888240	chr4:148830675-148830676	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1529936	chr4:148830679-148830680	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs1529937	chr4:148830680-148830681	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560247132	chr4:148830708-148830709	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1529939	chr4:148830728-148830729	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543654382	chr4:148830763-148830764	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113140448	chr4:148830765-148830766	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188602817	chr4:148830789-148830790	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552847319	chr4:148830793-148830794	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527688091	chr4:148830794-148830795	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551952204	chr4:148830807-148830808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77939149	chr4:148830850-148830851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377190962	chr4:148830860-148830861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548299896	chr4:148830907-148830908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373859702	chr4:148830951-148830952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537148854	chr4:148830962-148830963	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570044046	chr4:148830982-148830983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557153159	chr4:148831012-148831013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570642894	chr4:148831056-148831057	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148826925	chr4:148831065-148831066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4627844	chr4:148831070-148831071	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs78283456	chr4:148831075-148831076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181432165	chr4:148831095-148831096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554639649	chr4:148831114-148831115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371707136	chr4:148831167-148831168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542626932	chr4:148831168-148831169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574544009	chr4:148831221-148831222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561603819	chr4:148831264-148831265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543517415	chr4:148831321-148831322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375888578	chr4:148831341-148831342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114419241	chr4:148831349-148831350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186954839	chr4:148831353-148831354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191389473	chr4:148831363-148831364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560037686	chr4:148831366-148831367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528074898	chr4:148831428-148831429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116563052	chr4:148831454-148831455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568074577	chr4:148831457-148831458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182006105	chr4:148831462-148831463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576510397	chr4:148831500-148831501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544103138	chr4:148831501-148831502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs397790338	chr4:148831512-148831513	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148786000-148861400	Weak transcription	Pancreas	Pancrea
2	chr4:148796800-148863200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr4:148796800-148866000	Weak transcription	Thymus	Thymus
4	chr4:148797000-148834200	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr4:148797000-148835800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr4:148797400-148879600	Weak transcription	Gastric	stomach
7	chr4:148804600-148854400	Weak transcription	Psoas Muscle	Psoas
8	chr4:148820600-148833400	Weak transcription	Left Ventricle	heart
9	chr4:148820600-148861200	Weak transcription	Esophagus	oesophagus
10	chr4:148820800-148848800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr4:148823400-148836600	Weak transcription	Placenta	Placenta
12	chr4:148823600-148831600	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr4:148823600-148833400	Weak transcription	Fetal Stomach	stomach
14	chr4:148823600-148833800	Weak transcription	NHLF	lung
15	chr4:148823600-148834600	Weak transcription	Fetal Intestine Large	intestine
16	chr4:148824400-148831000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:148824400-148842800	Weak transcription	Lung	lung
18	chr4:148824400-148854600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr4:148824600-148854400	Weak transcription	Right Ventricle	heart
20	chr4:148824800-148833400	Weak transcription	Fetal Intestine Small	intestine
21	chr4:148825000-148834000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr4:148825000-148836200	Weak transcription	HMEC	breast
23	chr4:148825200-148831600	Weak transcription	Colon Smooth Muscle	Colon
24	chr4:148825200-148834000	Weak transcription	NHDF-Ad	bronchial
25	chr4:148825200-148835400	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr4:148825200-148839600	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr4:148825200-148847400	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr4:148825200-148848400	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr4:148825400-148832000	Weak transcription	Fetal Muscle Leg	muscle
30	chr4:148825400-148832400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr4:148825400-148834000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr4:148825400-148834000	Weak transcription	Osteobl	bone
33	chr4:148825400-148843400	Weak transcription	Fetal Heart	heart
34	chr4:148825400-148844200	Weak transcription	Duodenum Mucosa	Duodenum
35	chr4:148825400-148846200	Weak transcription	Fetal Kidney	kidney
36	chr4:148825400-148861200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr4:148825400-148865800	Weak transcription	Fetal Lung	lung
38	chr4:148826600-148888200	Weak transcription	Fetal Thymus	thymus
39	chr4:148827200-148832000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr4:148827200-148832800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr4:148827400-148861200	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr4:148827600-148831200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr4:148827800-148830800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr4:148827800-148832200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr4:148828200-148832000	Strong transcription	Adipose Nuclei	Adipose
46	chr4:148828400-148834200	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr4:148828400-148836400	Strong transcription	Aorta	Aorta
48	chr4:148828800-148831600	Weak transcription	HUVEC	blood vessel
49	chr4:148828800-148831800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr4:148829000-148834600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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