Variant report

Variant	nsv999754
Chromosome Location	chr4:3900840-4099676
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2597)
CpG islands
(count:1529)
Chromatin interactive
region (count:4)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2597 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:4053587-4053756	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:3956305-3956527	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:3956277-3956631	K562	blood:	n/a	n/a
4	ARID3A	chr4:4032212-4032597	K562	blood:	n/a	n/a
5	ARID3A	chr4:4039051-4039302	K562	blood:	n/a	n/a
6	ARID3A	chr4:4091843-4091964	HepG2	liver:	n/a	n/a
7	ATF1	chr4:3956318-3956561	K562	blood:	n/a	n/a
8	ATF1	chr4:3939560-3939786	K562	blood:	n/a	n/a
9	ATF1	chr4:3957144-3957802	K562	blood:	n/a	n/a
10	ATF1	chr4:4028563-4028766	K562	blood:	n/a	n/a
11	ATF2	chr4:4030515-4030906	GM12878	blood:	n/a	n/a
12	ATF2	chr4:4030551-4030873	GM12878	blood:	n/a	n/a
13	ATF2	chr4:4008103-4008392	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr4:4008126-4008444	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr4:4008194-4008377	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr4:3956235-3956568	K562	blood:	n/a	n/a
17	ATF3	chr4:4028561-4028781	K562	blood:	n/a	n/a
18	BATF	chr4:3951669-3951946	GM12878	blood:	n/a	n/a
19	BATF	chr4:3955991-3956766	GM12878	blood:	n/a	chr4:3956402-3956413 chr4:3956403-3956413
20	BATF	chr4:4027325-4027653	GM12878	blood:	n/a	chr4:4027432-4027440
21	BATF	chr4:4062237-4062520	GM12878	blood:	n/a	n/a
22	BATF	chr4:4010220-4010483	GM12878	blood:	n/a	n/a
23	BATF	chr4:3956028-3956299	GM12878	blood:	n/a	n/a
24	BATF	chr4:3941568-3941786	GM12878	blood:	n/a	n/a
25	BATF	chr4:4034090-4034531	GM12878	blood:	n/a	n/a
26	BATF	chr4:4030562-4030894	GM12878	blood:	n/a	n/a
27	BATF	chr4:4083071-4083386	GM12878	blood:	n/a	n/a
28	BATF	chr4:4034756-4035076	GM12878	blood:	n/a	n/a
29	BATF	chr4:4034951-4035173	GM12878	blood:	n/a	n/a
30	BATF	chr4:4031048-4031245	GM12878	blood:	n/a	n/a
31	BATF	chr4:4010229-4010487	GM12878	blood:	n/a	n/a
32	BATF	chr4:4095210-4095471	GM12878	blood:	n/a	n/a
33	BATF	chr4:4040204-4040389	GM12878	blood:	n/a	n/a
34	BATF	chr4:3956920-3957168	GM12878	blood:	n/a	n/a
35	BATF	chr4:3986537-3986888	GM12878	blood:	n/a	n/a
36	BATF	chr4:4083302-4083622	GM12878	blood:	n/a	n/a
37	BATF	chr4:4054755-4055203	GM12878	blood:	n/a	n/a
38	BATF	chr4:3939612-3939927	GM12878	blood:	n/a	n/a
39	BATF	chr4:4034092-4034580	GM12878	blood:	n/a	n/a
40	BATF	chr4:3986555-3986823	GM12878	blood:	n/a	n/a
41	BATF	chr4:4029216-4029487	GM12878	blood:	n/a	n/a
42	BATF	chr4:4083081-4083266	GM12878	blood:	n/a	n/a
43	BATF	chr4:3939526-3939933	GM12878	blood:	n/a	n/a
44	BATF	chr4:3944161-3944477	GM12878	blood:	n/a	n/a
45	BATF	chr4:4030502-4030972	GM12878	blood:	n/a	n/a
46	BATF	chr4:4062221-4062552	GM12878	blood:	n/a	n/a
47	BCL11A	chr4:4083377-4083668	GM12878	blood:	n/a	n/a
48	BCL11A	chr4:4030466-4031001	GM12878	blood:	n/a	chr4:4030940-4030949
49	BCL11A	chr4:4010216-4010510	GM12878	blood:	n/a	n/a
50	BCL11A	chr4:3944113-3944431	GM12878	blood:	n/a	n/a

(count:1529 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3949662-3949712	NT2-D1	testis:	n/a
2	chr4:3953675-3953725	SKMC	muscle:	n/a
3	chr4:3957584-3957634	AoSMC	blood vessel:	n/a
4	chr4:4050335-4050385	Caco-2	colon:	n/a
5	chr4:3949662-3949712	NT2-D1	testis:	n/a
6	chr4:3953675-3953725	SKMC	muscle:	n/a
7	chr4:3957584-3957634	AoSMC	blood vessel:	n/a
8	chr4:4050335-4050385	Caco-2	colon:	n/a
9	chr4:3949662-3949712	HEK293	kidney:	embryo
10	chr4:4022850-4022900	AG04450	lung:	fetal
11	chr4:4050335-4050385	NH-A	brain:	n/a
12	chr4:4034611-4034661	AoSMC	blood vessel:	n/a
13	chr4:3956448-3956498	HRPEpiC	eye:	n/a
14	chr4:3956772-3956822	SKMC	muscle:	n/a
15	chr4:3956448-3956498	HepG2	liver:	n/a
16	chr4:3960266-3960316	Jurkat	blood:	n/a
17	chr4:4035958-4036008	HCF	heart:	n/a
18	chr4:3957672-3957722	HRPEpiC	eye:	n/a
19	chr4:3956963-3957013	HPAEpiC	pulmonary alveolar:	n/a
20	chr4:3960266-3960316	BJ	skin:	n/a
21	chr4:3958437-3958487	ProgFib	skin:	n/a
22	chr4:3957584-3957634	K562	blood:	n/a
23	chr4:4034611-4034661	NB4	blood:	n/a
24	chr4:3957584-3957634	HRE	kidney:	n/a
25	chr4:4038806-4038856	HPAEpiC	pulmonary alveolar:	n/a
26	chr4:3960266-3960316	Caco-2	colon:	n/a
27	chr4:4022850-4022900	HCT-116	colon:	n/a
28	chr4:3956963-3957013	BE2_C	brain:	n/a
29	chr4:3956448-3956498	PFSK-1	brain:	n/a
30	chr4:3949662-3949712	AG09309	skin:	n/a
31	chr4:4022850-4022900	HCM	heart:	n/a
32	chr4:4050335-4050385	AG04449	skin:	fetal
33	chr4:4038659-4038709	ProgFib	skin:	n/a
34	chr4:4022850-4022900	ovcar-3	ovarian:	n/a
35	chr4:4034611-4034661	A549	lung:	n/a
36	chr4:4050309-4050359	AG09319	gingival:	n/a
37	chr4:4034611-4034661	HCT-116	colon:	n/a
38	chr4:3948537-3948587	IMR90	lung:	fetal
39	chr4:4034611-4034661	AG04449	skin:	fetal
40	chr4:3948578-3948628	PrEC	prostate:	n/a
41	chr4:3956448-3956498	U87	brain:	n/a
42	chr4:4034611-4034661	K562	blood:	n/a
43	chr4:4034611-4034661	HRCEpiC	kidney:	n/a
44	chr4:4049451-4049501	NHBE	bronchial:	n/a
45	chr4:3949662-3949712	SKMC	muscle:	n/a
46	chr4:3953675-3953725	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:3948537-3948587	HEK293	kidney:	embryo
48	chr4:3956772-3956822	SAEC	small airway:	n/a
49	chr4:3949662-3949712	K562	blood:	n/a
50	chr4:4049451-4049501	HCPEpiC	choroid plexus:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3481517..3483185-chr4:3946552..3949445,2	MCF-7	breast:
2	chr16:88717065..88717765-chr4:3956553..3957490,2	HCT-116	colon:
3	chr4:3952456..3954287-chr4:3955011..3957167,2	MCF-7	breast:
4	chr11:67572608..67573347-chr4:3956745..3957344,2	Hela-S3	cervix:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZBTB49-2	chr4:4043788-4043876	ENSG00000248614
2	lnc-OTOP1-6	chr4:3956687-3956728	NONHSAT094909
3	lnc-ZBTB49-2	chr4:4075923-4076780	ENSG00000248614
4	lnc-ZBTB49-2	chr4:4038040-4038211	ENSG00000248614
5	lnc-OTOP1-6	chr4:3944759-3945099	NONHSAT094909
6	lnc-OTOP1-4	chr4:4051761-4051909	NONHSAT094915
7	lnc-ADRA2C-1	chr4:3912010-3912331	NONHSAT094899
8	lnc-OTOP1-6	chr4:3954838-3954900	NONHSAT094909
9	lnc-ZBTB49-2	chr4:4040656-4040739	ENSG00000248614
10	lnc-ZBTB49-2	chr4:4034897-4034910	ENSG00000248614
11	lnc-OTOP1-6	chr4:3952866-3952946	NONHSAT094909

No data

Variant related genes	Relation type
ENSG00000253917	TF binding region
ENSG00000250940	TF binding region
ENSG00000249522	TF binding region
ENSG00000271977	TF binding region
ENSG00000264106	TF binding region
FAM86EP	TF binding region
ENPP7P9	TF binding region
OR7E162P	TF binding region
ENSG00000243894	TF binding region
ENSG00000221301	TF binding region
ALG1L7P	TF binding region
ENSG00000253917	CpG island
ENSG00000250940	CpG island
ENSG00000249522	CpG island
ENSG00000271977	CpG island
ENSG00000264106	CpG island
FAM86EP	CpG island
ENPP7P9	CpG island
OR7E162P	CpG island
ENSG00000243894	CpG island
ENSG00000221301	CpG island
ALG1L7P	CpG island
ENSG00000253917	chromatin interactions
ENSG00000251669	chromatin interactions
ENSG00000160172	chromatin interactions
ENSG00000051523	chromatin interactions

Extended variants
information (count: 9418 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:9418 , 50 per page) page: 1 2 3 4 5 6 7 ... 189

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536862487	chr4:3900841-3900842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs550235402	chr4:3900842-3900843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73792791	chr4:3900865-3900866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567002095	chr4:3900873-3900874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142771787	chr4:3900906-3900907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146077115	chr4:3900923-3900924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187266395	chr4:3900927-3900928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533847238	chr4:3900965-3900966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191783115	chr4:3900970-3900971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140102310	chr4:3900974-3900975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371021751	chr4:3901000-3901001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575765035	chr4:3901001-3901002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs62289204	chr4:3901002-3901003	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs28617372	chr4:3901010-3901011	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs183908044	chr4:3901033-3901034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35441866	chr4:3901036-3901037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540773609	chr4:3901067-3901068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537490694	chr4:3901084-3901085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572980679	chr4:3901092-3901093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533716735	chr4:3901099-3901100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188010017	chr4:3901142-3901143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565055795	chr4:3901153-3901154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188396972	chr4:3901165-3901166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs62289205	chr4:3901171-3901172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192273903	chr4:3901183-3901184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550347948	chr4:3901219-3901220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556416447	chr4:3901229-3901230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201168603	chr4:3901243-3901244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529737691	chr4:3901247-3901248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150886998	chr4:3901253-3901254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566424391	chr4:3901272-3901273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs28465628	chr4:3901273-3901274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558550908	chr4:3901279-3901280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569554963	chr4:3901307-3901308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538579455	chr4:3901310-3901311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555197951	chr4:3901326-3901327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575086928	chr4:3901346-3901347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540678965	chr4:3901355-3901356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553988606	chr4:3901356-3901357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372895099	chr4:3901364-3901365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543815713	chr4:3901367-3901368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs28588517	chr4:3901387-3901388	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs185865139	chr4:3901405-3901406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368121983	chr4:3901409-3901410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs28491663	chr4:3901413-3901414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560272545	chr4:3901414-3901415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35305857	chr4:3901418-3901419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs28460824	chr4:3901420-3901421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560703735	chr4:3901422-3901423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529848875	chr4:3901436-3901437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	18438408	CNVD
Ependymoma	20639864	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1120 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3896000-3905000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:3897200-3903800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:3898200-3906400	Weak transcription	Placenta	Placenta
4	chr4:3898600-3906400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr4:3903600-3904200	Enhancers	NHDF-Ad	bronchial
6	chr4:3903600-3904800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr4:3903800-3904200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:3903800-3904200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr4:3904200-3905000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr4:3904200-3906400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr4:3904200-3906400	Weak transcription	NHDF-Ad	bronchial
12	chr4:3904800-3905600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr4:3905000-3905200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr4:3905000-3905200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:3905000-3906400	Enhancers	Muscle Satellite Cultured Cells	--
16	chr4:3905000-3907200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr4:3905200-3906400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:3905200-3907200	Enhancers	Osteobl	bone
19	chr4:3905200-3913000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:3905600-3906400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr4:3905600-3906400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr4:3905600-3906800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:3905600-3907000	Enhancers	HSMMtube	muscle
24	chr4:3905600-3907600	Enhancers	HSMM	muscle
25	chr4:3906400-3906600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr4:3906400-3906800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr4:3906400-3906800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr4:3906400-3906800	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr4:3906400-3906800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
30	chr4:3906400-3907000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr4:3906400-3907000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
32	chr4:3906400-3907200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr4:3906400-3907200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr4:3906400-3907200	Enhancers	Placenta	Placenta
35	chr4:3906400-3907200	Enhancers	NH-A	brain
36	chr4:3906400-3907200	Enhancers	NHDF-Ad	bronchial
37	chr4:3906600-3906800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr4:3906600-3906800	Enhancers	Adipose Nuclei	Adipose
39	chr4:3906800-3907200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr4:3906800-3907200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr4:3906800-3907200	Enhancers	Muscle Satellite Cultured Cells	--
42	chr4:3906800-3907400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:3907200-3911200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr4:3907200-3911200	Weak transcription	NHDF-Ad	bronchial
45	chr4:3907200-3911800	Weak transcription	Placenta	Placenta
46	chr4:3907200-3912800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr4:3907400-3912000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr4:3911200-3912000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr4:3911200-3913600	Enhancers	NHDF-Ad	bronchial
50	chr4:3911400-3912200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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