Variant report

Variant	nsv997656
Chromosome Location	chr4:3909535-4120743
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2899)
CpG islands
(count:2319)
Chromatin interactive
region (count:4)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2899 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:3956305-3956527	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:4053587-4053756	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:4091843-4091964	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:4039051-4039302	K562	blood:	n/a	n/a
5	ARID3A	chr4:4032212-4032597	K562	blood:	n/a	n/a
6	ARID3A	chr4:3956277-3956631	K562	blood:	n/a	n/a
7	ATF1	chr4:3957144-3957802	K562	blood:	n/a	n/a
8	ATF1	chr4:3939560-3939786	K562	blood:	n/a	n/a
9	ATF1	chr4:3956318-3956561	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	chr4:4118748-4118905	K562	blood:	n/a	n/a
17	ATF3	chr4:4028561-4028781	K562	blood:	n/a	n/a
18	ATF3	chr4:3956235-3956568	K562	blood:	n/a	n/a
19	BACH1	chr4:4109215-4109581	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr4:4083071-4083386	GM12878	blood:	n/a	n/a
21	BATF	chr4:4027325-4027653	GM12878	blood:	n/a	chr4:4027432-4027440
22	BATF	chr4:4040204-4040389	GM12878	blood:	n/a	n/a
23	BATF	chr4:4083081-4083266	GM12878	blood:	n/a	n/a
24	BATF	chr4:4031048-4031245	GM12878	blood:	n/a	n/a
25	BATF	chr4:4062237-4062520	GM12878	blood:	n/a	n/a
26	BATF	chr4:4010220-4010483	GM12878	blood:	n/a	n/a
27	BATF	chr4:4030502-4030972	GM12878	blood:	n/a	n/a
28	BATF	chr4:4029216-4029487	GM12878	blood:	n/a	n/a
29	BATF	chr4:3939526-3939933	GM12878	blood:	n/a	n/a
30	BATF	chr4:4034092-4034580	GM12878	blood:	n/a	n/a
31	BATF	chr4:3955991-3956766	GM12878	blood:	n/a	chr4:3956402-3956413 chr4:3956403-3956413
32	BATF	chr4:3944161-3944477	GM12878	blood:	n/a	n/a
33	BATF	chr4:4034951-4035173	GM12878	blood:	n/a	n/a
34	BATF	chr4:4083302-4083622	GM12878	blood:	n/a	n/a
35	BATF	chr4:4054755-4055203	GM12878	blood:	n/a	n/a
36	BATF	chr4:4034756-4035076	GM12878	blood:	n/a	n/a
37	BATF	chr4:3939612-3939927	GM12878	blood:	n/a	n/a
38	BATF	chr4:4034090-4034531	GM12878	blood:	n/a	n/a
39	BATF	chr4:4030562-4030894	GM12878	blood:	n/a	n/a
40	BATF	chr4:3956920-3957168	GM12878	blood:	n/a	n/a
41	BATF	chr4:3951669-3951946	GM12878	blood:	n/a	n/a
42	BATF	chr4:3941568-3941786	GM12878	blood:	n/a	n/a
43	BATF	chr4:3956028-3956299	GM12878	blood:	n/a	n/a
44	BATF	chr4:3986537-3986888	GM12878	blood:	n/a	n/a
45	BATF	chr4:4062221-4062552	GM12878	blood:	n/a	n/a
46	BATF	chr4:3986555-3986823	GM12878	blood:	n/a	n/a
47	BATF	chr4:4095210-4095471	GM12878	blood:	n/a	n/a
48	BATF	chr4:4010229-4010487	GM12878	blood:	n/a	n/a
49	BCL11A	chr4:3955287-3955742	GM12878	blood:	n/a	n/a
50	BCL11A	chr4:4030466-4031001	GM12878	blood:	n/a	chr4:4030940-4030949

(count:2319 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3956448-3956498	A549	lung:	n/a
2	chr4:3956448-3956498	A549	lung:	n/a
3	chr4:4119674-4119724	SAEC	small airway:	n/a
4	chr4:4038725-4038775	GM19239	blood:	n/a
5	chr4:4105725-4105775	RPTEC	kidney:	n/a
6	chr4:3956772-3956822	Jurkat	blood:	n/a
7	chr4:4050309-4050359	GM06990	blood:	n/a
8	chr4:4050309-4050359	Hela-S3	cervix:	n/a
9	chr4:4109441-4109491	HPAEpiC	pulmonary alveolar:	n/a
10	chr4:4119674-4119724	HRE	kidney:	n/a
11	chr4:3957665-3957715	Jurkat	blood:	n/a
12	chr4:4038659-4038709	SK-N-SH_RA	brain:	n/a
13	chr4:3956963-3957013	AG09309	skin:	n/a
14	chr4:4038806-4038856	ECC-1	luminal epithelium:	n/a
15	chr4:4111130-4111180	SK-N-SH_RA	brain:	n/a
16	chr4:3957665-3957715	HCF	heart:	n/a
17	chr4:4109441-4109491	CMK	blood:	n/a
18	chr4:3960266-3960316	Jurkat	blood:	n/a
19	chr4:4034861-4034911	RPTEC	kidney:	n/a
20	chr4:4049816-4049866	HIPEpiC	eye:	n/a
21	chr4:4109441-4109491	Jurkat	blood:	n/a
22	chr4:3956772-3956822	BJ	skin:	n/a
23	chr4:4111130-4111180	PrEC	prostate:	n/a
24	chr4:4108791-4108841	Hepatocyte	liver:	n/a
25	chr4:4105725-4105775	AoSMC	blood vessel:	n/a
26	chr4:4049816-4049866	NH-A	brain:	n/a
27	chr4:3948537-3948587	HL-60	blood:	n/a
28	chr4:3960332-3960382	AG09309	skin:	n/a
29	chr4:3957584-3957634	NB4	blood:	n/a
30	chr4:4109446-4109496	NHBE	bronchial:	n/a
31	chr4:4034861-4034911	ovcar-3	ovarian:	n/a
32	chr4:4038659-4038709	AG09309	skin:	n/a
33	chr4:4049451-4049501	SAEC	small airway:	n/a
34	chr4:4034611-4034661	T-47D	breast:	n/a
35	chr4:3948578-3948628	NHBE	bronchial:	n/a
36	chr4:4117213-4117263	GM12892	blood:	n/a
37	chr4:3958437-3958487	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:4034861-4034911	ECC-1	luminal epithelium:	n/a
39	chr4:4120246-4120296	HCT-116	colon:	n/a
40	chr4:4049451-4049501	PFSK-1	brain:	n/a
41	chr4:4038659-4038709	IMR90	lung:	fetal
42	chr4:4109446-4109496	T-47D	breast:	n/a
43	chr4:4049816-4049866	GM19239	blood:	n/a
44	chr4:4107978-4108028	HCPEpiC	choroid plexus:	n/a
45	chr4:4049816-4049866	ECC-1	luminal epithelium:	n/a
46	chr4:4105725-4105775	SK-N-SH	brain:	n/a
47	chr4:3948578-3948628	HAEpiC	amniotic membrane:	n/a
48	chr4:4119945-4119995	ovcar-3	ovarian:	n/a
49	chr4:4022850-4022900	SAEC	small airway:	n/a
50	chr4:4108947-4108997	AG10803	skin:	n/a

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OTOP1-4	chr4:4051761-4051909	NONHSAT094915
2	lnc-OTOP1-4	chr4:4109007-4109306	NONHSAT094915
3	lnc-ZBTB49-2	chr4:4034897-4034910	ENSG00000248614
4	lnc-ZBTB49-2	chr4:4040656-4040739	ENSG00000248614
5	lnc-OTOP1-6	chr4:3954838-3954900	NONHSAT094909
6	lnc-ADRA2C-1	chr4:3912010-3912331	NONHSAT094899
7	lnc-ZBTB49-2	chr4:4043788-4043876	ENSG00000248614
8	lnc-OTOP1-6	chr4:3956687-3956728	NONHSAT094909
9	lnc-ZBTB49-2	chr4:4038040-4038211	ENSG00000248614
10	lnc-ZBTB49-2	chr4:4075923-4076780	ENSG00000248614
11	lnc-OTOP1-6	chr4:3944759-3945099	NONHSAT094909
12	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
ENSG00000264106	TF binding region
FAM86EP	TF binding region
ENSG00000248669	TF binding region
ENPP7P9	TF binding region
ENSG00000221301	TF binding region
ENSG00000271977	TF binding region
ENSG00000243894	TF binding region
ALG1L7P	TF binding region
ENSG00000253917	CpG island
ENSG00000250940	CpG island
ENSG00000249522	CpG island
ENSG00000264106	CpG island
FAM86EP	CpG island
ENSG00000248669	CpG island
ENPP7P9	CpG island
ENSG00000221301	CpG island
ENSG00000271977	CpG island
ENSG00000243894	CpG island
ALG1L7P	CpG island
ENSG00000160172	chromatin interactions
ENSG00000251669	chromatin interactions
ENSG00000253917	chromatin interactions
ENSG00000051523	chromatin interactions

Extended variants
information (count: 9462 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:9462 , 50 per page) page: 1 2 3 4 5 6 7 ... 190

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529078287	chr4:3909535-3909536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs548784247	chr4:3909542-3909543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541775227	chr4:3909552-3909553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570765994	chr4:3909568-3909569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145288645	chr4:3909569-3909570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112319327	chr4:3909582-3909583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113775143	chr4:3909620-3909621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141698746	chr4:3909629-3909630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112867057	chr4:3909631-3909632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73205011	chr4:3909633-3909634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551284755	chr4:3909637-3909638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572665058	chr4:3909641-3909642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs28420552	chr4:3909642-3909643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs367607674	chr4:3909645-3909646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140615259	chr4:3909655-3909656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372174800	chr4:3909667-3909668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184863178	chr4:3909669-3909670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573326608	chr4:3909681-3909682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539180574	chr4:3909701-3909702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558668765	chr4:3909707-3909708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189243410	chr4:3909719-3909720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192150504	chr4:3909725-3909726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs114699954	chr4:3909729-3909730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371546946	chr4:3909730-3909731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573609970	chr4:3909731-3909732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376633364	chr4:3909733-3909734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150542552	chr4:3909757-3909758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559171080	chr4:3909770-3909771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112410950	chr4:3909775-3909776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149300682	chr4:3909805-3909806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564705805	chr4:3909811-3909812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374485747	chr4:3909812-3909813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540918912	chr4:3909834-3909835	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs184993338	chr4:3909847-3909848	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs567918467	chr4:3909862-3909863	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs144604265	chr4:3909863-3909864	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs547211906	chr4:3909865-3909866	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs567109077	chr4:3909881-3909882	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs28539617	chr4:3909882-3909883	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs559035421	chr4:3909915-3909916	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs573881572	chr4:3909921-3909922	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs114566810	chr4:3909940-3909941	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs538200691	chr4:3909947-3909948	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs34419203	chr4:3909964-3909965	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs573597341	chr4:3909969-3909970	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs189872119	chr4:3909977-3909978	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs552734993	chr4:3909978-3909979	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs181144842	chr4:3909983-3909984	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs544897666	chr4:3909986-3909987	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs564959183	chr4:3910026-3910027	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:1233 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3905200-3913000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:3907200-3911200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr4:3907200-3911200	Weak transcription	NHDF-Ad	bronchial
4	chr4:3907200-3911800	Weak transcription	Placenta	Placenta
5	chr4:3907200-3912800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:3907400-3912000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr4:3911200-3912000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:3911200-3913600	Enhancers	NHDF-Ad	bronchial
9	chr4:3911400-3912200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr4:3911800-3912600	Enhancers	Placenta	Placenta
11	chr4:3911800-3913000	Enhancers	Fetal Heart	heart
12	chr4:3912000-3912400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr4:3912000-3912600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr4:3912000-3913000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr4:3912200-3912800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr4:3912200-3913400	Enhancers	Adipose Nuclei	Adipose
17	chr4:3912400-3916200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:3912600-3912800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr4:3912600-3913000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr4:3912800-3913000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr4:3912800-3913200	Bivalent/Poised TSS	Fetal Brain Male	brain
22	chr4:3912800-3913400	ZNF genes & repeats	Fetal Kidney	kidney
23	chr4:3912800-3913600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr4:3912800-3913600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr4:3912800-3913600	Bivalent/Poised TSS	Fetal Lung	lung
26	chr4:3913000-3913200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr4:3913000-3913200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr4:3913000-3913200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr4:3913000-3913200	Bivalent Enhancer	Fetal Heart	heart
30	chr4:3913000-3913400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr4:3913000-3913600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
32	chr4:3913000-3913600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:3913000-3920600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr4:3913200-3913600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr4:3913200-3914200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr4:3913600-3913800	Weak transcription	Fetal Kidney	kidney
37	chr4:3913600-3916200	Weak transcription	NHDF-Ad	bronchial
38	chr4:3913600-3923600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr4:3913600-3928600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr4:3913600-3928600	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr4:3914200-3914400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr4:3914600-3914800	Enhancers	Osteobl	bone
43	chr4:3914800-3916400	Weak transcription	Osteobl	bone
44	chr4:3916000-3916600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr4:3916000-3916600	Enhancers	Brain Anterior Caudate	brain
46	chr4:3916200-3916600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr4:3916200-3917000	Enhancers	NHDF-Ad	bronchial
48	chr4:3916400-3916800	Enhancers	Osteobl	bone
49	chr4:3916600-3921200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr4:3916800-3921000	Weak transcription	Osteobl	bone

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