Variant report

Variant	nsv879826
Chromosome Location	chr4:118292314-118351381
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	BACH1	chr4:118323436-118323468	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr4:118321267-118321684	HCT-116	colon:	n/a	chr4:118321304-118321315
3	CEBPB	chr4:118339135-118339335	IMR90	lung:	n/a	n/a
4	CEBPB	chr4:118333928-118334149	H1-hESC	embryonic stem cell:	n/a	chr4:118334008-118334019
5	CEBPB	chr4:118341771-118341971	A549	lung:	n/a	chr4:118341866-118341877 chr4:118341891-118341902 chr4:118341866-118341879 chr4:118341868-118341877 chr4:118341867-118341878 chr4:118341868-118341877 chr4:118341868-118341877 chr4:118341868-118341877
6	CEBPB	chr4:118321302-118321657	IMR90	lung:	n/a	n/a
7	CEBPB	chr4:118338686-118338912	IMR90	lung:	n/a	n/a
8	CEBPB	chr4:118333852-118334143	A549	lung:	n/a	chr4:118334008-118334019
9	CEBPB	chr4:118314143-118314469	IMR90	lung:	n/a	n/a
10	CEBPB	chr4:118333842-118334173	K562	blood:	n/a	chr4:118334008-118334019
11	CEBPB	chr4:118341725-118342029	HepG2	liver:	n/a	chr4:118341866-118341877 chr4:118341891-118341902 chr4:118341866-118341879 chr4:118341868-118341877 chr4:118341867-118341878 chr4:118341868-118341877 chr4:118341868-118341877 chr4:118341868-118341877
12	CEBPB	chr4:118323728-118323964	IMR90	lung:	n/a	chr4:118323852-118323865 chr4:118323852-118323863 chr4:118323803-118323820 chr4:118323852-118323865 chr4:118323805-118323816 chr4:118323852-118323863 chr4:118323853-118323864 chr4:118323852-118323865 chr4:118323768-118323785
13	CEBPB	chr4:118333829-118334187	IMR90	lung:	n/a	chr4:118334008-118334019
14	CEBPB	chr4:118333846-118334182	HepG2	liver:	n/a	chr4:118334008-118334019
15	CEBPB	chr4:118338078-118338345	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:118323695-118323971	HepG2	liver:	n/a	chr4:118323852-118323865 chr4:118323852-118323863 chr4:118323803-118323820 chr4:118323852-118323865 chr4:118323805-118323816 chr4:118323852-118323863 chr4:118323853-118323864 chr4:118323852-118323865 chr4:118323768-118323785
17	CTCF	chr4:118350340-118350490	GM12873	blood:	n/a	n/a
18	CTCF	chr4:118313702-118314051	MCF-7	breast:	n/a	n/a
19	CTCF	chr4:118350340-118350490	GM12874	blood:	n/a	n/a
20	CTCF	chr4:118350312-118350361	Fibrobl	skin:	n/a	n/a
21	CTCF	chr4:118350359-118350503	GM12878	blood:	n/a	n/a
22	CTCF	chr4:118350360-118350510	BE2_C	brain:	n/a	n/a
23	CTCF	chr4:118350261-118350614	GM12878	blood:	n/a	n/a
24	CTCF	chr4:118350347-118350525	GM12892	blood:	n/a	n/a
25	CTCF	chr4:118350380-118350530	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr4:118350340-118350490	GM12869	blood:	n/a	n/a
27	CTCF	chr4:118350520-118350670	RPTEC	kidney:	n/a	n/a
28	CTCF	chr4:118350352-118350523	GM19240	blood:	n/a	n/a
29	CTCF	chr4:118350360-118350510	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr4:118350300-118350450	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr4:118313762-118313952	MCF-7	breast:	n/a	n/a
32	CTCF	chr4:118350440-118350590	AG04450	lung:	n/a	n/a
33	CTCF	chr4:118350380-118350530	GM12878	blood:	n/a	n/a
34	CTCF	chr4:118350335-118350486	HepG2	liver:	n/a	n/a
35	CTCF	chr4:118350380-118350530	A549	lung:	n/a	n/a
36	CTCF	chr4:118350367-118350465	MCF-7	breast:	n/a	n/a
37	CTCF	chr4:118313760-118313910	HepG2	liver:	n/a	n/a
38	CTCF	chr4:118350323-118350539	GM19238	blood:	n/a	n/a
39	CTCF	chr4:118350340-118350490	HPF	lung:	n/a	n/a
40	CTCF	chr4:118350340-118350490	GM12868	blood:	n/a	n/a
41	CTCF	chr4:118350380-118350530	NHEK	skin:	n/a	n/a
42	CTCF	chr4:118350380-118350530	HepG2	liver:	n/a	n/a
43	CTCF	chr4:118350480-118350630	BE2_C	brain:	n/a	n/a
44	CTCF	chr4:118350300-118350450	HEK293	kidney:	n/a	n/a
45	CTCF	chr4:118350400-118350550	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr4:118350402-118350469	HepG2	liver:	n/a	n/a
47	CTCF	chr4:118350340-118350490	HCT-116	colon:	n/a	n/a
48	CTCF	chr4:118350380-118350530	GM12864	blood:	n/a	n/a
49	CTCF	chr4:118350400-118350550	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr4:118350400-118350550	HBMEC	blood vessel:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	4:118320200-118324249..4:118414019-118416561	Hela-S3	cervix:
2	4:118319405-118319911..4:118559839-118566258	H1-hESC	embryonic stem cell:	embryo
3	4:118301798-118302725..4:118541860-118551269	H1-hESC	embryonic stem cell:	embryo
4	4:118291537-118294071..4:118722741-118723956	H1-hESC	embryonic stem cell:	embryo
5	4:118313000-118315008..4:118319405-118319911	H1-hESC	embryonic stem cell:	embryo
6	4:118319405-118319911..4:118687551-118689447	H1-hESC	embryonic stem cell:	embryo
7	4:118312235-118312291..4:118319405-118319911	H1-hESC	embryonic stem cell:	embryo
8	4:118320200-118324249..4:118722741-118723956	H1-hESC	embryonic stem cell:	embryo
9	4:118320200-118324249..4:118559839-118566258	GM12878	blood:
10	4:118319405-118319911..4:118454469-118464115	H1-hESC	embryonic stem cell:	embryo
11	4:118312235-118312291..4:118636913-118638401	H1-hESC	embryonic stem cell:	embryo
12	4:118320200-118324249..4:118735152-118737645	GM12878	blood:
13	4:118327401-118331084..4:118559839-118566258	GM12878	blood:
14	4:118312235-118312291..4:118319405-118319911	H1-hESC	embryonic stem cell:	embryo
15	4:118313000-118315008..4:118319405-118319911	H1-hESC	embryonic stem cell:	embryo
16	4:118291537-118294071..4:118559839-118566258	H1-hESC	embryonic stem cell:	embryo

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDST3-5	chr4:118293520-118293627	XLOC_003658
2	lnc-NDST3-5	chr4:118292748-118292818	XLOC_003658
3	lnc-NDST3-5	chr4:118292748-118292818	XLOC_003658
4	lnc-NDST3-5	chr4:118292748-118292818	XLOC_003658
5	lnc-NDST3-5	chr4:118292748-118292818	XLOC_003658
6	lnc-NDST3-5	chr4:118292748-118292818	XLOC_003658
7	lnc-NDST3-4	chr4:118349850-118349923	ENSG00000236922
8	lnc-NDST3-4	chr4:118349559-118349639	ENSG00000236922
9	lnc-NDST3-5	chr4:118293914-118294008	XLOC_003658
10	lnc-NDST3-5	chr4:118293520-118293627	XLOC_003658
11	lnc-NDST3-5	chr4:118293520-118293891	XLOC_003658
12	lnc-NDST3-5	chr4:118292748-118292818	XLOC_003658
13	lnc-NDST3-10	chr4:118334618-118335435	NONHSAT097958
14	lnc-NDST3-5	chr4:118293752-118293891	XLOC_003658
15	lnc-NDST3-4	chr4:118349552-118349639	ENSG00000236922.5
16	lnc-NDST3-5	chr4:118293752-118293858	XLOC_003658
17	lnc-NDST3-5	chr4:118293520-118293627	XLOC_003658
18	lnc-NDST3-5	chr4:118293914-118293973	XLOC_003658
19	lnc-NDST3-4	chr4:118349853-118349923	ENSG00000236922.5
20	lnc-NDST3-5	chr4:118293520-118293754	XLOC_003658
21	lnc-NDST3-5	chr4:118293520-118293627	XLOC_003658

Variant related genes	Relation type
ENSG00000236922	TF binding region
RPSAP35	TF binding region
ARID3B	miRNA target sites
EIF4G2	miRNA target sites
KIAA0528	miRNA target sites

Extended variants
information (count: 1791 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1791 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3925016	chr4:118292314-118292315	Enhancers Strong transcription Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144165742	chr4:118292354-118292355	Enhancers Strong transcription Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185248414	chr4:118292419-118292420	Enhancers Strong transcription Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549953896	chr4:118292454-118292455	Enhancers Strong transcription Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569962869	chr4:118292465-118292466	Enhancers Strong transcription Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538900682	chr4:118292499-118292500	Enhancers Strong transcription Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145936109	chr4:118292511-118292512	Enhancers Strong transcription Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531884663	chr4:118292574-118292575	Enhancers Strong transcription Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577533421	chr4:118292642-118292643	Enhancers Strong transcription Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533577490	chr4:118292649-118292650	Enhancers Strong transcription Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553761864	chr4:118292690-118292691	Enhancers Strong transcription Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs17861808	chr4:118292709-118292710	Enhancers Strong transcription Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs556996077	chr4:118292716-118292717	Enhancers Strong transcription Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542788381	chr4:118292734-118292735	Enhancers Strong transcription Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148623400	chr4:118292826-118292827	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs17861809	chr4:118292890-118292891	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs545288132	chr4:118292898-118292899	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs17866829	chr4:118292950-118292951	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs189044140	chr4:118293012-118293013	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547459302	chr4:118293026-118293027	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561375296	chr4:118293042-118293043	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs17861188	chr4:118293077-118293078	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181827696	chr4:118293139-118293140	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142088676	chr4:118293149-118293150	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569875555	chr4:118293160-118293161	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537674277	chr4:118293192-118293193	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538878736	chr4:118293197-118293198	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369883295	chr4:118293198-118293199	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148442358	chr4:118293209-118293210	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545516729	chr4:118293218-118293219	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs17869651	chr4:118293220-118293221	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs17865069	chr4:118293296-118293297	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs17861810	chr4:118293332-118293333	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs553908909	chr4:118293339-118293340	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535339212	chr4:118293369-118293370	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553445162	chr4:118293528-118293529	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs376237931	chr4:118293537-118293538	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs186425343	chr4:118293550-118293551	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs369422854	chr4:118293556-118293557	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs17869541	chr4:118293591-118293592	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs17861811	chr4:118293651-118293652	Strong transcription Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs557063561	chr4:118293682-118293683	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs141142384	chr4:118293683-118293684	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs17861812	chr4:118293690-118293691	Strong transcription Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs545196193	chr4:118293713-118293714	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs565104222	chr4:118293772-118293773	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs188140957	chr4:118293783-118293784	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs541320713	chr4:118293799-118293800	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs561122300	chr4:118293829-118293830	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs530075014	chr4:118293835-118293836	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	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
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Autism	19246517	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:118282000-118302000	Weak transcription	HMEC	breast
2	chr4:118292200-118292800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:118292200-118292800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr4:118292200-118292800	Active TSS	Brain Inferior Temporal Lobe	brain
5	chr4:118292200-118295800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:118294000-118294400	Enhancers	Fetal Brain Male	brain
7	chr4:118294400-118297400	Weak transcription	Fetal Brain Male	brain
8	chr4:118295800-118306200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:118297400-118297800	Enhancers	Fetal Brain Male	brain
10	chr4:118302000-118302400	Enhancers	HMEC	breast
11	chr4:118303800-118304600	Weak transcription	Fetal Brain Male	brain
12	chr4:118304600-118306000	Enhancers	Fetal Brain Male	brain
13	chr4:118306000-118307200	Weak transcription	Fetal Brain Male	brain
14	chr4:118306200-118307200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr4:118306600-118307800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr4:118306800-118307200	Enhancers	Brain Anterior Caudate	brain
17	chr4:118307000-118307600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:118307200-118307600	Enhancers	Fetal Brain Male	brain
19	chr4:118307200-118308000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr4:118307200-118309200	Weak transcription	Brain Anterior Caudate	brain
21	chr4:118307200-118321000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr4:118309200-118309800	Enhancers	Brain Anterior Caudate	brain
23	chr4:118309400-118309600	Enhancers	Fetal Brain Male	brain
24	chr4:118313800-118322200	Weak transcription	Pancreas	Pancrea
25	chr4:118320600-118321000	Enhancers	HSMM	muscle
26	chr4:118320600-118321000	Enhancers	HUVEC	blood vessel
27	chr4:118320800-118321000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr4:118320800-118321000	Enhancers	Dnd41	blood
29	chr4:118320800-118321200	Enhancers	NH-A	brain
30	chr4:118321000-118321400	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr4:118321000-118321400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr4:118321000-118321400	Active TSS	Brain Cingulate Gyrus	brain
33	chr4:118321000-118321400	Enhancers	HMEC	breast
34	chr4:118321000-118321400	Flanking Active TSS	HSMM	muscle
35	chr4:118321000-118321600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr4:118321000-118321600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr4:118321000-118321600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr4:118321000-118321600	Flanking Active TSS	Dnd41	blood
39	chr4:118321000-118321600	Flanking Active TSS	HUVEC	blood vessel
40	chr4:118321000-118321600	Active TSS	Osteobl	bone
41	chr4:118321000-118321800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr4:118321000-118321800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr4:118321000-118321800	Enhancers	NHEK	skin
44	chr4:118321200-118321400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr4:118321200-118321400	Enhancers	Brain Hippocampus Middle	brain
46	chr4:118321200-118321600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr4:118321200-118321600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:118321200-118321600	Enhancers	Brain Angular Gyrus	brain
49	chr4:118321200-118321600	Flanking Active TSS	NH-A	brain
50	chr4:118321200-118322200	Enhancers	Muscle Satellite Cultured Cells	--

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