Variant report

Variant	nsv4540
Chromosome Location	chr4:148230593-148275778
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	BATF	chr4:148261839-148262240	GM12878	blood:	n/a	n/a
2	BATF	chr4:148261867-148262233	GM12878	blood:	n/a	n/a
3	BCL11A	chr4:148261742-148262052	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:148261694-148262154	GM12878	blood:	n/a	n/a
5	CBX3	chr4:148261189-148262132	HCT-116	colon:	n/a	n/a
6	CEBPB	chr4:148272260-148273163	HCT-116	colon:	n/a	chr4:148272450-148272461
7	CEBPB	chr4:148272284-148273134	IMR90	lung:	n/a	chr4:148272450-148272461
8	CEBPB	chr4:148261346-148261634	IMR90	lung:	n/a	n/a
9	CEBPB	chr4:148272323-148272603	K562	blood:	n/a	chr4:148272450-148272461
10	CEBPB	chr4:148272317-148272564	A549	lung:	n/a	chr4:148272450-148272461
11	CEBPB	chr4:148233519-148233836	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr4:148233509-148233820	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:148272222-148272948	Hela-S3	cervix:	n/a	chr4:148272450-148272461
14	CEBPB	chr4:148268040-148268290	HepG2	liver:	n/a	chr4:148268181-148268192
15	CEBPB	chr4:148272310-148272570	HepG2	liver:	n/a	chr4:148272450-148272461
16	CTCF	chr4:148230720-148230870	HCPEpiC	choroid plexus:	n/a	chr4:148230786-148230799
17	CTCF	chr4:148246680-148246830	NHDF-neo	bronchial:	n/a	n/a
18	CTCF	chr4:148269810-148269916	Lung_OC	lung:	n/a	n/a
19	CTCF	chr4:148246660-148246810	AG10803	skin:	n/a	n/a
20	CTCF	chr4:148272100-148272250	HPF	lung:	n/a	n/a
21	CTCF	chr4:148249668-148249719	GM20000	blood:	n/a	n/a
22	CTCF	chr4:148260270-148260326	Fibrobl	skin:	n/a	n/a
23	CTCF	chr4:148230749-148230829	Lung_OC	lung:	n/a	chr4:148230786-148230799
24	CTCF	chr4:148230740-148230890	HCPEpiC	choroid plexus:	n/a	chr4:148230786-148230799
25	E2F4	chr4:148248500-148248631	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr4:148272432-148272814	MCF10A-Er-Src	breast:	n/a	n/a
27	EBF1	chr4:148261732-148262174	GM12878	blood:	n/a	n/a
28	EP300	chr4:148246677-148247141	SK-N-SH_RA	brain:	n/a	chr4:148247130-148247140
29	EP300	chr4:148247743-148248072	SK-N-SH_RA	brain:	n/a	n/a
30	EP300	chr4:148261201-148262579	SK-N-SH	brain:	n/a	chr4:148261482-148261491
31	EP300	chr4:148233085-148233486	SK-N-SH_RA	brain:	n/a	n/a
32	EP300	chr4:148264865-148265178	SK-N-SH_RA	brain:	n/a	chr4:148265025-148265034 chr4:148265149-148265163 chr4:148265026-148265035
33	EP300	chr4:148261024-148263036	SK-N-SH	brain:	n/a	chr4:148261116-148261130 chr4:148262818-148262832 chr4:148261482-148261491 chr4:148262816-148262830 chr4:148263008-148263022
34	EP300	chr4:148260134-148260707	SK-N-SH_RA	brain:	n/a	n/a
35	EP300	chr4:148246655-148247246	SK-N-SH_RA	brain:	n/a	chr4:148247130-148247140
36	EP300	chr4:148255449-148255997	SK-N-SH_RA	brain:	n/a	chr4:148255728-148255737 chr4:148255776-148255790 chr4:148255773-148255787 chr4:148255820-148255829
37	EP300	chr4:148232995-148234001	SK-N-SH	brain:	n/a	chr4:148233757-148233767 chr4:148233764-148233773
38	EP300	chr4:148261126-148261644	SK-N-SH_RA	brain:	n/a	chr4:148261482-148261491
39	EP300	chr4:148260261-148260649	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr4:148261674-148262560	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr4:148261674-148262454	SK-N-SH_RA	brain:	n/a	n/a
42	FAM48A	chr4:148257129-148257280	GM12878	blood:	n/a	n/a
43	FOS	chr4:148264890-148265180	MCF10A-Er-Src	breast:	n/a	chr4:148265026-148265034 chr4:148265022-148265033 chr4:148265024-148265035 chr4:148265024-148265036 chr4:148265025-148265035 chr4:148265027-148265034 chr4:148265025-148265034 chr4:148265026-148265035
44	FOS	chr4:148264933-148265133	MCF10A-Er-Src	breast:	n/a	chr4:148265026-148265034 chr4:148265022-148265033 chr4:148265024-148265035 chr4:148265024-148265036 chr4:148265025-148265035 chr4:148265027-148265034 chr4:148265025-148265034 chr4:148265026-148265035
45	FOS	chr4:148261142-148262084	HUVEC	blood vessel:	n/a	chr4:148261481-148261491 chr4:148261482-148261490 chr4:148261480-148261491 chr4:148262070-148262082 chr4:148261765-148261773 chr4:148261482-148261490 chr4:148261481-148261491 chr4:148261481-148261491 chr4:148261481-148261491 chr4:148261483-148261494 chr4:148261482-148261489
46	FOS	chr4:148255522-148255980	HUVEC	blood vessel:	n/a	chr4:148255726-148255737 chr4:148255728-148255736 chr4:148255728-148255735 chr4:148255728-148255737
47	FOS	chr4:148250395-148250507	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr4:148261318-148261666	MCF10A-Er-Src	breast:	n/a	chr4:148261481-148261491 chr4:148261482-148261490 chr4:148261480-148261491 chr4:148261482-148261490 chr4:148261481-148261491 chr4:148261481-148261491 chr4:148261481-148261491 chr4:148261483-148261494 chr4:148261482-148261489
49	FOS	chr4:148261330-148261656	MCF10A-Er-Src	breast:	n/a	chr4:148261481-148261491 chr4:148261482-148261490 chr4:148261480-148261491 chr4:148261482-148261490 chr4:148261481-148261491 chr4:148261481-148261491 chr4:148261481-148261491 chr4:148261483-148261494 chr4:148261482-148261489
50	FOS	chr4:148255637-148255789	MCF10A-Er-Src	breast:	n/a	chr4:148255726-148255737 chr4:148255728-148255736 chr4:148255728-148255735 chr4:148255728-148255737

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:148254941-148254991	SK-N-SH	brain:	n/a
2	chr4:148254941-148254991	SK-N-SH	brain:	n/a
3	chr4:148233162-148233212	HepG2	liver:	n/a
4	chr4:148254941-148254991	MCF10A-Er-Src	breast:	n/a
5	chr4:148260510-148260560	GM06990	blood:	n/a
6	chr4:148260510-148260560	SK-N-SH_RA	brain:	n/a
7	chr4:148260510-148260560	NT2-D1	testis:	n/a
8	chr4:148233162-148233212	A549	lung:	n/a
9	chr4:148254941-148254991	HCT-116	colon:	n/a
10	chr4:148254941-148254991	NT2-D1	testis:	n/a
11	chr4:148233162-148233212	Jurkat	blood:	n/a
12	chr4:148260510-148260560	HL-60	blood:	n/a
13	chr4:148260510-148260560	Hela-S3	cervix:	n/a
14	chr4:148254941-148254991	ECC-1	luminal epithelium:	n/a
15	chr4:148233162-148233212	RPTEC	kidney:	n/a
16	chr4:148254941-148254991	AG09319	gingival:	n/a
17	chr4:148233162-148233212	SK-N-MC	brain:	n/a
18	chr4:148260510-148260560	NB4	blood:	n/a
19	chr4:148260510-148260560	Caco-2	colon:	n/a
20	chr4:148260510-148260560	HEEpiC	esophagus:	n/a
21	chr4:148260510-148260560	AG09309	skin:	n/a
22	chr4:148254941-148254991	GM12878	blood:	n/a
23	chr4:148233162-148233212	AG10803	skin:	n/a
24	chr4:148254941-148254991	NB4	blood:	n/a
25	chr4:148254941-148254991	HRCEpiC	kidney:	n/a
26	chr4:148254941-148254991	BJ	skin:	n/a
27	chr4:148260510-148260560	T-47D	breast:	n/a
28	chr4:148254941-148254991	SK-N-SH_RA	brain:	n/a
29	chr4:148254941-148254991	HCF	heart:	n/a
30	chr4:148254941-148254991	ProgFib	skin:	n/a
31	chr4:148233162-148233212	Hepatocyte	liver:	n/a
32	chr4:148233162-148233212	BJ	skin:	n/a
33	chr4:148254941-148254991	H1-hESC	embryonic stem cell:	embryo
34	chr4:148233162-148233212	ECC-1	luminal epithelium:	n/a
35	chr4:148260510-148260560	GM12891	blood:	n/a
36	chr4:148254941-148254991	NH-A	brain:	n/a
37	chr4:148260510-148260560	SK-N-SH	brain:	n/a
38	chr4:148254941-148254991	AG10803	skin:	n/a
39	chr4:148260510-148260560	HCM	heart:	n/a
40	chr4:148233162-148233212	HEK293	kidney:	embryo
41	chr4:148260510-148260560	SK-N-MC	brain:	n/a
42	chr4:148233162-148233212	HCM	heart:	n/a
43	chr4:148260510-148260560	GM12892	blood:	n/a
44	chr4:148233162-148233212	T-47D	breast:	n/a
45	chr4:148260510-148260560	K562	blood:	n/a
46	chr4:148233162-148233212	NB4	blood:	n/a
47	chr4:148260510-148260560	PFSK-1	brain:	n/a
48	chr4:148233162-148233212	MCF-7	breast:	n/a
49	chr4:148233162-148233212	SK-N-SH	brain:	n/a
50	chr4:148233162-148233212	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:148272436..148274239-chr4:148281813..148283538,2	MCF-7	breast:
2	chr4:148229582..148231427-chr4:148235135..148238116,2	K562	blood:
3	chr4:148229582..148231427-chr4:148235135..148238116,2	K562	blood:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548g-5p	chr4:148265833-148265855	MIMAT0022722
hsa-miR-548g-3p	chr4:148265795-148265816	MIMAT0005912

Variant related genes	Relation type
MIR548G	TF binding region
MIR548G	CpG island

Extended variants
information (count: 1590 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574026830	chr4:148230599-148230600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542929046	chr4:148230612-148230613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs35043015	chr4:148230678-148230679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562701685	chr4:148230716-148230717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183501549	chr4:148230754-148230755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575887839	chr4:148230756-148230757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545190125	chr4:148230789-148230790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370846192	chr4:148230808-148230809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528672262	chr4:148230852-148230853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543314069	chr4:148230878-148230879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527331985	chr4:148230932-148230933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375669391	chr4:148230958-148230959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547124886	chr4:148230965-148230966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561519724	chr4:148231054-148231055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148524663	chr4:148231056-148231057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35964958	chr4:148231065-148231066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573295923	chr4:148231078-148231079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530358941	chr4:148231162-148231163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368454296	chr4:148231197-148231198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550037158	chr4:148231268-148231269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371506650	chr4:148231290-148231291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569984799	chr4:148231321-148231322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142801274	chr4:148231399-148231400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552693660	chr4:148231530-148231531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566089914	chr4:148231533-148231534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs77692603	chr4:148231534-148231535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554702384	chr4:148231615-148231616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs151026364	chr4:148231631-148231632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537414986	chr4:148231652-148231653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188546142	chr4:148231657-148231658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142339016	chr4:148231694-148231695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544877770	chr4:148231706-148231707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147844554	chr4:148231818-148231819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568756746	chr4:148231838-148231839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192490704	chr4:148231879-148231880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141370268	chr4:148231892-148231893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560575308	chr4:148231935-148231936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529236713	chr4:148231952-148231953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375947819	chr4:148231954-148231955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549330472	chr4:148232040-148232041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146974901	chr4:148232056-148232057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs183393135	chr4:148232092-148232093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186613387	chr4:148232096-148232097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191136406	chr4:148232120-148232121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566251677	chr4:148232126-148232127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs114464177	chr4:148232136-148232137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368781579	chr4:148232147-148232148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568533375	chr4:148232217-148232218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530753626	chr4:148232284-148232285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs183685128	chr4:148232434-148232435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Intellectual disability	22102821	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
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	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
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	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
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:219 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148229400-148230600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr4:148230000-148233000	Weak transcription	Fetal Kidney	kidney
3	chr4:148230400-148230600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:148230400-148230800	Enhancers	Fetal Heart	heart
5	chr4:148230600-148231400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr4:148230600-148233600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr4:148231400-148232000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr4:148231600-148234200	Enhancers	Adipose Nuclei	Adipose
9	chr4:148231800-148232000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:148232000-148233600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr4:148232200-148233200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr4:148232600-148234600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr4:148232800-148233200	Weak transcription	A549	lung
14	chr4:148232800-148234600	Enhancers	Fetal Stomach	stomach
15	chr4:148233000-148233600	Enhancers	Fetal Lung	lung
16	chr4:148233000-148234200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr4:148233000-148234600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr4:148233000-148234600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr4:148233000-148234600	Enhancers	Ovary	ovary
20	chr4:148233000-148235200	Enhancers	Fetal Kidney	kidney
21	chr4:148233200-148233400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr4:148233200-148233400	Enhancers	A549	lung
23	chr4:148233200-148234400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr4:148233200-148234600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr4:148233200-148235200	Enhancers	Hela-S3	cervix
26	chr4:148233400-148235200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr4:148233600-148233800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:148233600-148234200	Enhancers	H9 Cell Line	embryonic stem cell
29	chr4:148233600-148234200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr4:148233600-148234200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr4:148233600-148234400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr4:148233600-148235200	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr4:148233600-148237800	Weak transcription	Fetal Lung	lung
34	chr4:148233800-148234200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr4:148233800-148234200	Enhancers	HSMM	muscle
36	chr4:148233800-148234400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr4:148234200-148234800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr4:148234200-148237800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:148234200-148239600	Weak transcription	Adipose Nuclei	Adipose
40	chr4:148234400-148239400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr4:148234600-148239200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr4:148234600-148240000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr4:148234600-148247800	Weak transcription	Fetal Stomach	stomach
44	chr4:148234800-148235000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr4:148235200-148237800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr4:148235200-148239600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr4:148235200-148239800	Weak transcription	Fetal Kidney	kidney
48	chr4:148236800-148237800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr4:148237800-148238000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:148237800-148238200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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