Variant report

Variant	esv1802846
Chromosome Location	chr4:88211056-88246450
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:247)
CpG islands
(count:366)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:247 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:88238747-88239287	HepG2	liver:	n/a	n/a
2	ATF2	chr4:88227219-88227557	GM12878	blood:	n/a	n/a
3	ATF2	chr4:88227105-88227643	GM12878	blood:	n/a	n/a
4	ATF3	chr4:88223744-88223892	K562	blood:	n/a	n/a
5	BATF	chr4:88227243-88227499	GM12878	blood:	n/a	chr4:88227386-88227397
6	BATF	chr4:88228029-88228308	GM12878	blood:	n/a	n/a
7	BCL3	chr4:88225796-88226325	A549	lung:	n/a	n/a
8	BCL3	chr4:88227213-88227544	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:88238776-88238949	HepG2	liver:	n/a	n/a
10	BRCA1	chr4:88225715-88226363	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr4:88215016-88215405	K562	blood:	n/a	n/a
12	CEBPB	chr4:88226731-88227502	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr4:88225700-88226496	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr4:88238721-88239017	A549	lung:	n/a	n/a
15	CEBPB	chr4:88238687-88239062	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:88238773-88238946	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:88238169-88239081	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr4:88238667-88239136	MCF-7	breast:	n/a	n/a
19	CEBPB	chr4:88238748-88239007	A549	lung:	n/a	n/a
20	CEBPB	chr4:88222910-88223189	K562	blood:	n/a	chr4:88223035-88223046
21	CEBPB	chr4:88238754-88238999	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:88241858-88242058	K562	blood:	n/a	chr4:88241967-88241980 chr4:88241967-88241978
23	CEBPB	chr4:88241820-88242139	HepG2	liver:	n/a	chr4:88241967-88241980 chr4:88241967-88241978
24	CEBPB	chr4:88238743-88239106	MCF-7	breast:	n/a	n/a
25	CEBPB	chr4:88222884-88223200	IMR90	lung:	n/a	chr4:88223035-88223046
26	CEBPB	chr4:88222879-88223179	HepG2	liver:	n/a	chr4:88223035-88223046
27	CEBPB	chr4:88238650-88239170	A549	lung:	n/a	n/a
28	CEBPB	chr4:88222901-88223173	A549	lung:	n/a	chr4:88223035-88223046
29	CEBPB	chr4:88230065-88230288	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr4:88225791-88226474	MCF-7	breast:	n/a	n/a
31	CEBPD	chr4:88238790-88238923	HepG2	liver:	n/a	n/a
32	CREB1	chr4:88227197-88227666	GM12878	blood:	n/a	n/a
33	CTCF	chr4:88222500-88222650	GM12873	blood:	n/a	n/a
34	CTCF	chr4:88244499-88244534	GM10266	blood:	n/a	n/a
35	CTCF	chr4:88246397-88246473	GM13976	blood:	n/a	n/a
36	CTCF	chr4:88231984-88232030	K562	blood:	n/a	n/a
37	CTCF	chr4:88213449-88213554	Lung_OC	lung:	n/a	n/a
38	CTCF	chr4:88229638-88229837	K562	blood:	n/a	n/a
39	CTCF	chr4:88231972-88232092	HepG2	liver:	n/a	n/a
40	CTCF	chr4:88236142-88236207	Lung_OC	lung:	n/a	n/a
41	CTCF	chr4:88232018-88232044	Hela-S3	cervix:	n/a	n/a
42	E2F4	chr4:88216610-88216698	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr4:88224694-88224894	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr4:88238529-88238892	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr4:88240482-88240682	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr4:88238119-88238310	MCF10A-Er-Src	breast:	n/a	n/a
47	EP300	chr4:88225710-88226470	A549	lung:	n/a	n/a
48	EP300	chr4:88238820-88238936	HepG2	liver:	n/a	n/a
49	EP300	chr4:88225710-88226451	A549	lung:	n/a	n/a
50	EP300	chr4:88238728-88239002	HepG2	liver:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:88244142-88244192	PFSK-1	brain:	n/a
2	chr4:88244142-88244192	ovcar-3	ovarian:	n/a
3	chr4:88243818-88243868	SAEC	small airway:	n/a
4	chr4:88244142-88244192	SK-N-MC	brain:	n/a
5	chr4:88244909-88244959	Caco-2	colon:	n/a
6	chr4:88244909-88244959	MCF-7	breast:	n/a
7	chr4:88245032-88245082	SAEC	small airway:	n/a
8	chr4:88244909-88244959	Hela-S3	cervix:	n/a
9	chr4:88225834-88225884	ECC-1	luminal epithelium:	n/a
10	chr4:88245032-88245082	BJ	skin:	n/a
11	chr4:88243818-88243868	ECC-1	luminal epithelium:	n/a
12	chr4:88243818-88243868	BE2_C	brain:	n/a
13	chr4:88245032-88245082	HMEC	breast:	n/a
14	chr4:88233933-88233983	NHDF-neo	bronchial:	n/a
15	chr4:88243818-88243868	Caco-2	colon:	n/a
16	chr4:88233933-88233983	GM12878	blood:	n/a
17	chr4:88244142-88244192	AG10803	skin:	n/a
18	chr4:88244909-88244959	SK-N-SH	brain:	n/a
19	chr4:88243818-88243868	SKMC	muscle:	n/a
20	chr4:88225834-88225884	AG04450	lung:	fetal
21	chr4:88233933-88233983	NB4	blood:	n/a
22	chr4:88243818-88243868	U87	brain:	n/a
23	chr4:88233933-88233983	ECC-1	luminal epithelium:	n/a
24	chr4:88243818-88243868	NT2-D1	testis:	n/a
25	chr4:88245032-88245082	NHBE	bronchial:	n/a
26	chr4:88244909-88244959	HAEpiC	amniotic membrane:	n/a
27	chr4:88233933-88233983	CMK	blood:	n/a
28	chr4:88244909-88244959	BJ	skin:	n/a
29	chr4:88225834-88225884	HCT-116	colon:	n/a
30	chr4:88225834-88225884	BE2_C	brain:	n/a
31	chr4:88243818-88243868	AG10803	skin:	n/a
32	chr4:88244909-88244959	HRE	kidney:	n/a
33	chr4:88244909-88244959	ovcar-3	ovarian:	n/a
34	chr4:88225834-88225884	HRPEpiC	eye:	n/a
35	chr4:88243818-88243868	MCF-7	breast:	n/a
36	chr4:88244142-88244192	U87	brain:	n/a
37	chr4:88233933-88233983	NT2-D1	testis:	n/a
38	chr4:88244142-88244192	A549	lung:	n/a
39	chr4:88245032-88245082	HAEpiC	amniotic membrane:	n/a
40	chr4:88233933-88233983	NHBE	bronchial:	n/a
41	chr4:88244142-88244192	K562	blood:	n/a
42	chr4:88243818-88243868	H1-hESC	embryonic stem cell:	embryo
43	chr4:88243818-88243868	HIPEpiC	eye:	n/a
44	chr4:88243818-88243868	NHBE	bronchial:	n/a
45	chr4:88244142-88244192	HPAEpiC	pulmonary alveolar:	n/a
46	chr4:88244142-88244192	HCM	heart:	n/a
47	chr4:88244909-88244959	T-47D	breast:	n/a
48	chr4:88233933-88233983	SK-N-SH_RA	brain:	n/a
49	chr4:88225834-88225884	NB4	blood:	n/a
50	chr4:88233933-88233983	GM06990	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:88226132..88228278-chr4:88229243..88230944,2	MCF-7	breast:
2	chr4:88229442..88232296-chr4:88234376..88236070,2	K562	blood:
3	chr4:88225790..88227669-chr4:88236912..88239118,2	MCF-7	breast:
4	chr4:88225790..88227669-chr4:88236912..88239118,2	MCF-7	breast:
5	chr4:88225793..88228433-chr4:88233021..88235909,2	MCF-7	breast:
6	chr4:88229442..88232296-chr4:88234376..88236070,2	K562	blood:
7	chr4:88216757..88219177-chr4:88220101..88221682,2	MCF-7	breast:
8	chr4:88224415..88227242-chr4:88231505..88233396,2	K562	blood:
9	chr4:88216757..88219177-chr4:88220101..88221682,2	MCF-7	breast:
10	chr4:88226132..88228278-chr4:88229243..88230944,2	MCF-7	breast:
11	chr4:88225793..88228433-chr4:88233021..88235909,2	MCF-7	breast:
12	chr4:88224415..88227242-chr4:88231505..88233396,2	K562	blood:
13	chr4:88237707..88239445-chr4:88243261..88245305,2	MCF-7	breast:
14	chr4:88187820..88189394-chr4:88231187..88233154,2	MCF-7	breast:
15	chr4:88141337..88143545-chr4:88209433..88211061,2	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5705	chr4:88221657-88221679	MIMAT0022499

No data

Variant related genes	Relation type
HSD17B13	TF binding region
MIR5705	TF binding region
HSD17B13	CpG island
MIR5705	CpG island
ENSG00000170509	chromatin interactions
ENSG00000145332	chromatin interactions
ENSG00000250572	chromatin interactions

Extended variants
information (count: 1044 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1044 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10084835	chr4:88211056-88211057	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114302507	chr4:88220804-88220805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4505787	chr4:88220835-88220836	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs190120538	chr4:88220837-88220838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs57455613	chr4:88220843-88220844	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs549036144	chr4:88220880-88220881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs558345611	chr4:88220934-88220935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs193218000	chr4:88220973-88220974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185633052	chr4:88221009-88221010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550232987	chr4:88221051-88221052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs75931587	chr4:88221106-88221107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538296495	chr4:88221136-88221137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs59054114	chr4:88221191-88221192	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs140168459	chr4:88221192-88221193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189260931	chr4:88221216-88221217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543908546	chr4:88221217-88221218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143918712	chr4:88221267-88221268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs180864924	chr4:88221303-88221304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs4079	chr4:88221318-88221319	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs185268235	chr4:88221331-88221332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs4089	chr4:88221345-88221346	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs540923514	chr4:88221364-88221365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188469544	chr4:88221428-88221429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146351376	chr4:88221433-88221434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181314077	chr4:88221446-88221447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542745729	chr4:88221466-88221467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139701132	chr4:88221489-88221490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531830122	chr4:88221510-88221511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550339302	chr4:88221541-88221542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565296125	chr4:88221560-88221561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142946358	chr4:88221579-88221580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186841994	chr4:88221585-88221586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565579229	chr4:88221592-88221593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76971307	chr4:88221632-88221633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542632345	chr4:88221664-88221665	Weak transcription	miRNA	n/a	Overlapped CNVs	n/a
36	rs191682972	chr4:88221709-88221710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183869804	chr4:88221748-88221749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs116111897	chr4:88221773-88221774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150954602	chr4:88221782-88221783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536709544	chr4:88221799-88221800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs62305716	chr4:88221817-88221818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187216339	chr4:88221836-88221837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113664973	chr4:88221838-88221839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544812868	chr4:88221918-88221919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs62305717	chr4:88221936-88221937	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs530540324	chr4:88221996-88221997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140793930	chr4:88222003-88222004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549272294	chr4:88222008-88222009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs115665918	chr4:88222014-88222015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4271972	chr4:88222065-88222066	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:82)

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
lymphocytic leukemia	21291569	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
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	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
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:88220800-88221400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:88221000-88221400	Enhancers	Liver	Liver
3	chr4:88221000-88221400	Enhancers	Fetal Lung	lung
4	chr4:88221400-88225400	Weak transcription	Liver	Liver
5	chr4:88221400-88225800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr4:88224000-88225600	Enhancers	Hela-S3	cervix
7	chr4:88225400-88237800	Strong transcription	Liver	Liver
8	chr4:88225600-88225800	Flanking Active TSS	Hela-S3	cervix
9	chr4:88225600-88225800	Enhancers	NHEK	skin
10	chr4:88225800-88226000	Enhancers	Osteobl	bone
11	chr4:88225800-88226200	Flanking Active TSS	NHEK	skin
12	chr4:88225800-88226400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:88225800-88226400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr4:88225800-88227200	Active TSS	Hela-S3	cervix
15	chr4:88226000-88226600	Active TSS	A549	lung
16	chr4:88226200-88226600	Active TSS	Aorta	Aorta
17	chr4:88226200-88226800	Active TSS	NHEK	skin
18	chr4:88226400-88231600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr4:88226600-88227000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr4:88226600-88229000	Weak transcription	A549	lung
21	chr4:88226800-88227200	Flanking Active TSS	NHEK	skin
22	chr4:88227000-88229000	Enhancers	Stomach Mucosa	stomach
23	chr4:88227200-88227600	Flanking Active TSS	Hela-S3	cervix
24	chr4:88227600-88228400	Enhancers	Hela-S3	cervix
25	chr4:88228000-88239600	Weak transcription	Primary hematopoietic stem cells	blood
26	chr4:88228400-88237800	Weak transcription	Hela-S3	cervix
27	chr4:88228800-88229000	Enhancers	Pancreas	Pancrea
28	chr4:88228800-88229000	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr4:88229000-88229200	Enhancers	A549	lung
30	chr4:88229000-88235600	Weak transcription	Pancreas	Pancrea
31	chr4:88229000-88245000	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr4:88229600-88235800	Weak transcription	Ovary	ovary
33	chr4:88230000-88230800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr4:88230000-88240000	Weak transcription	Brain Angular Gyrus	brain
35	chr4:88230200-88231000	Weak transcription	Left Ventricle	heart
36	chr4:88230200-88231200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr4:88230600-88231000	Enhancers	Osteobl	bone
38	chr4:88230600-88239600	Weak transcription	Primary T cells from cord blood	blood
39	chr4:88231000-88231400	Genic enhancers	Left Ventricle	heart
40	chr4:88231200-88235600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr4:88231400-88237400	Weak transcription	Left Ventricle	heart
42	chr4:88231600-88232600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:88231600-88233000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr4:88232200-88233400	Enhancers	Fetal Heart	heart
45	chr4:88232600-88233000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:88233000-88233400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:88234000-88235600	Weak transcription	Adipose Nuclei	Adipose
48	chr4:88234400-88237000	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr4:88235200-88243800	Weak transcription	Rectal Smooth Muscle	rectum
50	chr4:88235600-88235800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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