Variant report

Variant	nsv881390
Chromosome Location	chr4:167163302-167237947
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	CEBPB	chr4:167178506-167178746	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr4:167203362-167203933	Hela-S3	cervix:	n/a	chr4:167203686-167203699 chr4:167203686-167203699 chr4:167203686-167203699
3	CEBPB	chr4:167178451-167178706	IMR90	lung:	n/a	n/a
4	CEBPB	chr4:167178451-167178734	HepG2	liver:	n/a	n/a
5	CEBPB	chr4:167196005-167196311	K562	blood:	n/a	chr4:167196127-167196138 chr4:167196045-167196056 chr4:167196125-167196142 chr4:167196126-167196139
6	CEBPB	chr4:167195977-167196303	Hela-S3	cervix:	n/a	chr4:167196127-167196138 chr4:167196045-167196056 chr4:167196125-167196142 chr4:167196126-167196139
7	CEBPB	chr4:167195965-167196308	A549	lung:	n/a	chr4:167196127-167196138 chr4:167196045-167196056 chr4:167196125-167196142 chr4:167196126-167196139
8	CEBPB	chr4:167234208-167234481	HepG2	liver:	n/a	chr4:167234319-167234330
9	CEBPB	chr4:167234267-167234422	K562	blood:	n/a	chr4:167234319-167234330
10	CEBPB	chr4:167195962-167196307	HepG2	liver:	n/a	chr4:167196127-167196138 chr4:167196045-167196056 chr4:167196125-167196142 chr4:167196126-167196139
11	CEBPB	chr4:167195969-167196290	H1-hESC	embryonic stem cell:	n/a	chr4:167196127-167196138 chr4:167196045-167196056 chr4:167196125-167196142 chr4:167196126-167196139
12	CEBPB	chr4:167178473-167178631	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr4:167178471-167178706	A549	lung:	n/a	n/a
14	CEBPB	chr4:167201970-167202208	MCF-7	breast:	n/a	chr4:167202074-167202087
15	CEBPB	chr4:167221731-167221812	HepG2	liver:	n/a	chr4:167221750-167221761
16	CEBPB	chr4:167195952-167196306	IMR90	lung:	n/a	chr4:167196127-167196138 chr4:167196045-167196056 chr4:167196125-167196142 chr4:167196126-167196139
17	CTCF	chr4:167174040-167174190	HVMF	connective:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
18	CTCF	chr4:167174180-167174330	HAc	cerebellar:	n/a	n/a
19	CTCF	chr4:167174060-167174210	NHLF	lung:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
20	CTCF	chr4:167174120-167174270	HUVEC	blood vessel:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
21	CTCF	chr4:167174020-167174170	HL-60	blood:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
22	CTCF	chr4:167174060-167174210	AG04449	skin:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
23	CTCF	chr4:167174100-167174250	HCM	heart:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
24	CTCF	chr4:167174090-167174229	GM19238	blood:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
25	CTCF	chr4:167174066-167174227	Pancreas_OC	pancreas:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
26	CTCF	chr4:167174060-167174210	HRE	kidney:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
27	CTCF	chr4:167174120-167174270	NB4	blood:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
28	CTCF	chr4:167174080-167174230	GM12869	blood:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
29	CTCF	chr4:167173848-167174465	HCT-116	colon:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
30	CTCF	chr4:167174049-167174252	ProgFib	skin:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
31	CTCF	chr4:167174100-167174250	MCF-7	breast:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
32	CTCF	chr4:167173858-167174366	SK-N-SH	brain:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
33	CTCF	chr4:167174080-167174230	MCF-7	breast:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
34	CTCF	chr4:167174002-167174269	ECC-1	luminal epithelium:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
35	CTCF	chr4:167174120-167174270	AG04450	lung:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
36	CTCF	chr4:167174009-167174214	A549	lung:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
37	CTCF	chr4:167174060-167174210	AoAF	blood vessel:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
38	CTCF	chr4:167174080-167174230	GM12872	blood:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
39	CTCF	chr4:167174100-167174250	HCFaa	heart:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
40	CTCF	chr4:167173968-167174266	H1-hESC	embryonic stem cell:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
41	CTCF	chr4:167174060-167174210	GM12868	blood:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
42	CTCF	chr4:167174080-167174230	HPF	lung:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
43	CTCF	chr4:167174060-167174210	HMEC	breast:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
44	CTCF	chr4:167174080-167174230	BE2_C	brain:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
45	CTCF	chr4:167174060-167174210	HCPEpiC	choroid plexus:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
46	CTCF	chr4:167174060-167174210	Caco-2	colon:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
47	CTCF	chr4:167174020-167174170	GM06990	blood:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
48	CTCF	chr4:167174060-167174210	GM12873	blood:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
49	CTCF	chr4:167174060-167174210	GM12864	blood:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147
50	CTCF	chr4:167174080-167174230	AG09309	skin:	n/a	chr4:167174135-167174145 chr4:167174132-167174150 chr4:167174127-167174148 chr4:167174133-167174149 chr4:167174138-167174147

No.	Distal block	Cell Line	Cell type
1	chr4:167086659..167087619-chr4:167173764..167174746,5	MCF-7	breast:
2	chr4:167086669..167087587-chr4:167173432..167174252,3	MCF-7	breast:
3	chr2:198174852..198175582-chr4:167182637..167183400,2	HCT-116	colon:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPOCK3-5	chr4:167236991-167240148	predAs_chen_BG208718_1

Variant related genes	Relation type
ENSG00000206711	TF binding region
ENSG00000065413	chromatin interactions

Extended variants
information (count: 769 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:769 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371543946	chr4:167176216-167176217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs184955389	chr4:167176275-167176276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551996664	chr4:167176296-167176297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535702552	chr4:167176329-167176330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536219708	chr4:167176331-167176332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs6810473	chr4:167176340-167176341	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs569686296	chr4:167176359-167176360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs448538	chr4:167176371-167176372	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs548266752	chr4:167176394-167176395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539705936	chr4:167176395-167176396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs80190415	chr4:167176453-167176454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188107486	chr4:167176595-167176596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114836612	chr4:167176602-167176603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562075541	chr4:167176606-167176607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs371903316	chr4:167176622-167176623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs180955024	chr4:167176629-167176630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs375701262	chr4:167176631-167176632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541680654	chr4:167176640-167176641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563461981	chr4:167176652-167176653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534191620	chr4:167176660-167176661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142932857	chr4:167176684-167176685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116634478	chr4:167176743-167176744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555764487	chr4:167176757-167176758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562152871	chr4:167176822-167176823	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs374838542	chr4:167176824-167176825	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs528131620	chr4:167176834-167176835	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs1663600	chr4:167176845-167176846	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs151082853	chr4:167176851-167176852	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs535502758	chr4:167176933-167176934	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs550905988	chr4:167176944-167176945	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs569389652	chr4:167176952-167176953	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs143734175	chr4:167176986-167176987	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs184748918	chr4:167177009-167177010	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs71604434	chr4:167177019-167177020	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs558072653	chr4:167177034-167177035	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs1675024	chr4:167177046-167177047	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs7677325	chr4:167177101-167177102	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs74321766	chr4:167177102-167177103	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs537970548	chr4:167177112-167177113	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs373490872	chr4:167177129-167177130	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs554234802	chr4:167177149-167177150	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs56797805	chr4:167177173-167177174	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs574385032	chr4:167177189-167177190	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs146900238	chr4:167177190-167177191	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs368283523	chr4:167177206-167177207	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs546009594	chr4:167177207-167177208	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs564405504	chr4:167177216-167177217	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs147887869	chr4:167177231-167177232	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs546297414	chr4:167177254-167177255	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs78945941	chr4:167177316-167177317	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	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
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	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
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Glioblastoma multiforme	22286061	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	16774939	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
intellectual deficit	22127048	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:167176200-167176800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:167176800-167177400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:167179000-167179400	Enhancers	Placenta	Placenta
4	chr4:167184000-167184200	Bivalent Enhancer	Aorta	Aorta
5	chr4:167198200-167198800	Enhancers	Osteobl	bone
6	chr4:167198200-167199400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr4:167198400-167198800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr4:167198400-167199600	Enhancers	NH-A	brain
9	chr4:167198800-167199200	Weak transcription	Osteobl	bone
10	chr4:167199200-167199600	Enhancers	Osteobl	bone
11	chr4:167213000-167213400	Enhancers	HUVEC	blood vessel
12	chr4:167213400-167213800	Weak transcription	HUVEC	blood vessel
13	chr4:167213800-167215000	Enhancers	HUVEC	blood vessel
14	chr4:167214400-167214800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:167214400-167214800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr4:167214400-167215000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr4:167214400-167215000	Enhancers	Muscle Satellite Cultured Cells	--
18	chr4:167222000-167222400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr4:167222200-167222400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr4:167222200-167222400	Enhancers	NH-A	brain
21	chr4:167222400-167222800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr4:167222400-167223000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:167222600-167223000	Enhancers	Osteobl	bone
24	chr4:167222800-167223000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr4:167223000-167223200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr4:167223000-167223200	Enhancers	NH-A	brain
27	chr4:167226600-167230000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:167229000-167231200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr4:167229200-167230400	Enhancers	NHEK	skin
30	chr4:167229400-167231000	Enhancers	HMEC	breast
31	chr4:167229600-167230600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr4:167229800-167230000	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr4:167230000-167230800	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr4:167230000-167231200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:167230800-167231000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr4:167230800-167231000	Enhancers	Osteobl	bone
37	chr4:167230800-167231600	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr4:167231000-167231200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:167231000-167232600	Weak transcription	HMEC	breast
40	chr4:167231000-167232600	Weak transcription	Osteobl	bone
41	chr4:167231200-167232400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr4:167231200-167233000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr4:167231400-167232400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr4:167231600-167240600	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr4:167232400-167233400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr4:167232400-167233800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr4:167232600-167233200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr4:167232600-167233200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr4:167232600-167233200	Enhancers	Osteobl	bone
50	chr4:167232600-167233400	Enhancers	HMEC	breast

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