Variant report

Variant	nsv879020
Chromosome Location	chr4:54986912-55064573
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:365)
CpG islands
(count:183)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:365 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:55042506-55042682	HepG2	liver:	n/a	n/a
2	CEBPB	chr4:55031582-55032140	HCT-116	colon:	n/a	n/a
3	CEBPB	chr4:55052053-55052346	Hela-S3	cervix:	n/a	chr4:55052163-55052174
4	CEBPB	chr4:54986766-54987010	A549	lung:	n/a	chr4:54986874-54986885
5	CEBPB	chr4:54986704-54987025	HepG2	liver:	n/a	chr4:54986874-54986885
6	CEBPB	chr4:55056942-55057247	HepG2	liver:	n/a	chr4:55057103-55057114 chr4:55057103-55057116
7	CEBPB	chr4:55042515-55042763	HepG2	liver:	n/a	n/a
8	CEBPB	chr4:55047645-55047747	HepG2	liver:	n/a	chr4:55047718-55047729
9	CEBPB	chr4:55047581-55047752	K562	blood:	n/a	chr4:55047718-55047729
10	CEBPB	chr4:55017884-55018090	IMR90	lung:	n/a	n/a
11	CEBPB	chr4:55029489-55029824	IMR90	lung:	n/a	chr4:55029647-55029658
12	CEBPB	chr4:55029527-55029771	A549	lung:	n/a	chr4:55029647-55029658
13	CEBPB	chr4:55031401-55031999	IMR90	lung:	n/a	chr4:55031565-55031582
14	CEBPB	chr4:54986729-54987029	K562	blood:	n/a	chr4:54986874-54986885
15	CEBPB	chr4:55052122-55052239	K562	blood:	n/a	chr4:55052163-55052174
16	CEBPB	chr4:55029511-55029801	HepG2	liver:	n/a	chr4:55029647-55029658
17	CEBPB	chr4:55029503-55029784	K562	blood:	n/a	chr4:55029647-55029658
18	CEBPB	chr4:55047635-55047757	H1-hESC	embryonic stem cell:	n/a	chr4:55047718-55047729
19	CEBPB	chr4:55052002-55052283	HepG2	liver:	n/a	chr4:55052163-55052174
20	CEBPB	chr4:55059335-55059377	HepG2	liver:	n/a	chr4:55059348-55059359
21	CEBPB	chr4:55047567-55047808	IMR90	lung:	n/a	chr4:55047718-55047729
22	CEBPB	chr4:54986780-54986983	IMR90	lung:	n/a	chr4:54986874-54986885
23	CTCF	chr4:55031780-55031930	AG04450	lung:	n/a	n/a
24	CTCF	chr4:55031660-55031810	HPF	lung:	n/a	n/a
25	CTCF	chr4:55053620-55053770	HCM	heart:	n/a	n/a
26	CTCF	chr4:55059052-55059302	K562	blood:	n/a	n/a
27	CTCF	chr4:55031580-55031730	AG09319	gingival:	n/a	n/a
28	CTCF	chr4:55031760-55031910	NHDF-neo	bronchial:	n/a	n/a
29	CTCF	chr4:55031720-55031870	HEK293	kidney:	n/a	n/a
30	CTCF	chr4:55031499-55032058	IMR90	lung:	n/a	n/a
31	CTCF	chr4:55059096-55059233	NHEK	skin:	n/a	n/a
32	CTCF	chr4:55031640-55031790	AG09319	gingival:	n/a	n/a
33	CTCF	chr4:55031720-55031870	WI-38	lung:	n/a	n/a
34	CTCF	chr4:55059120-55059270	A549	lung:	n/a	n/a
35	CTCF	chr4:55031580-55031730	HVMF	connective:	n/a	n/a
36	CTCF	chr4:55059124-55059203	HepG2	liver:	n/a	n/a
37	CTCF	chr4:55031680-55031830	HPF	lung:	n/a	n/a
38	CTCF	chr4:55051690-55051802	A549	lung:	n/a	n/a
39	CTCF	chr4:55057860-55058010	HEK293	kidney:	n/a	n/a
40	CTCF	chr4:55053440-55053590	HCM	heart:	n/a	n/a
41	CTCF	chr4:55053440-55053590	HPF	lung:	n/a	n/a
42	CTCF	chr4:55031700-55031850	AG10803	skin:	n/a	n/a
43	CTCF	chr4:55005632-55005690	Medullo	brain:	n/a	n/a
44	CTCF	chr4:55058959-55059345	K562	blood:	n/a	n/a
45	CTCF	chr4:55031720-55031870	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr4:55051580-55051730	GM12873	blood:	n/a	n/a
47	CTCF	chr4:55051639-55051803	K562	blood:	n/a	n/a
48	CTCF	chr4:55063830-55063887	GM20000	blood:	n/a	n/a
49	CTCF	chr4:55059115-55059169	GM19238	blood:	n/a	n/a
50	CTCF	chr4:55051640-55051790	Hela-S3	cervix:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:55031503-55031553	GM12891	blood:	n/a
2	chr4:55063893-55063943	K562	blood:	n/a
3	chr4:55031503-55031553	BE2_C	brain:	n/a
4	chr4:55063893-55063943	GM12878	blood:	n/a
5	chr4:55031503-55031553	HRPEpiC	eye:	n/a
6	chr4:55019140-55019190	HRCEpiC	kidney:	n/a
7	chr4:55031503-55031553	Hepatocyte	liver:	n/a
8	chr4:55019140-55019190	MCF-7	breast:	n/a
9	chr4:55063893-55063943	HAEpiC	amniotic membrane:	n/a
10	chr4:55019140-55019190	CMK	blood:	n/a
11	chr4:55031503-55031553	AoSMC	blood vessel:	n/a
12	chr4:55019140-55019190	U87	brain:	n/a
13	chr4:55019140-55019190	HAEpiC	amniotic membrane:	n/a
14	chr4:55031503-55031553	MCF10A-Er-Src	breast:	n/a
15	chr4:55063893-55063943	HCPEpiC	choroid plexus:	n/a
16	chr4:55019140-55019190	Hepatocyte	liver:	n/a
17	chr4:55019140-55019190	SAEC	small airway:	n/a
18	chr4:55031503-55031553	HRCEpiC	kidney:	n/a
19	chr4:55031503-55031553	K562	blood:	n/a
20	chr4:55019140-55019190	A549	lung:	n/a
21	chr4:55019140-55019190	AG04450	lung:	fetal
22	chr4:55019140-55019190	GM12891	blood:	n/a
23	chr4:55063893-55063943	CMK	blood:	n/a
24	chr4:55031503-55031553	HRE	kidney:	n/a
25	chr4:55031503-55031553	IMR90	lung:	fetal
26	chr4:55031503-55031553	GM06990	blood:	n/a
27	chr4:55031503-55031553	AG09319	gingival:	n/a
28	chr4:55019140-55019190	HCF	heart:	n/a
29	chr4:55019140-55019190	HUVEC	blood vessel:	n/a
30	chr4:55063893-55063943	Hela-S3	cervix:	n/a
31	chr4:55063893-55063943	HEEpiC	esophagus:	n/a
32	chr4:55031503-55031553	HEK293	kidney:	embryo
33	chr4:55019140-55019190	AG04449	skin:	fetal
34	chr4:55063893-55063943	NHBE	bronchial:	n/a
35	chr4:55031503-55031553	AG09309	skin:	n/a
36	chr4:55019140-55019190	HCM	heart:	n/a
37	chr4:55063893-55063943	AG09319	gingival:	n/a
38	chr4:55063893-55063943	LNCaP	prostate:	n/a
39	chr4:55031503-55031553	NT2-D1	testis:	n/a
40	chr4:55063893-55063943	NB4	blood:	n/a
41	chr4:55063893-55063943	GM12891	blood:	n/a
42	chr4:55019140-55019190	SK-N-SH_RA	brain:	n/a
43	chr4:55019140-55019190	HEEpiC	esophagus:	n/a
44	chr4:55031503-55031553	BJ	skin:	n/a
45	chr4:55031503-55031553	SK-N-SH_RA	brain:	n/a
46	chr4:55031503-55031553	HCPEpiC	choroid plexus:	n/a
47	chr4:55031503-55031553	NHDF-neo	bronchial:	n/a
48	chr4:55019140-55019190	K562	blood:	n/a
49	chr4:55031503-55031553	A549	lung:	n/a
50	chr4:55019140-55019190	BE2_C	brain:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:55011296..55011796-chr9:131873114..131873945,2	Hela-S3	cervix:
2	chr4:54967560..54969215-chr4:55017035..55019730,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000238753	TF binding region
ENSG00000238753	CpG island
ENSG00000095321	chromatin interactions
ENSG00000119383	chromatin interactions

Extended variants
information (count: 1999 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1999 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6850083	chr4:54986912-54986913	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541327768	chr4:54987014-54987015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564812307	chr4:54987060-54987061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370362018	chr4:54987067-54987068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533318520	chr4:54987108-54987109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192034619	chr4:54987131-54987132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182257535	chr4:54987168-54987169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369621262	chr4:54987175-54987176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185996282	chr4:54987198-54987199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189672208	chr4:54987270-54987271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565909085	chr4:54987277-54987278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs373675299	chr4:54987303-54987304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182848110	chr4:54987404-54987405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs73252934	chr4:54987415-54987416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570720011	chr4:54987423-54987424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs139033641	chr4:54987485-54987486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370883550	chr4:54987489-54987490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576808025	chr4:54987506-54987507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539782436	chr4:54987588-54987589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185677325	chr4:54987610-54987611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569893383	chr4:54987616-54987617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535513378	chr4:54987670-54987671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555454852	chr4:54987728-54987729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114112969	chr4:54987729-54987730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542288068	chr4:54989607-54989608	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs570879707	chr4:54989615-54989616	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs536658865	chr4:54989617-54989618	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs557187276	chr4:54989646-54989647	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs547452407	chr4:54990726-54990727	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs542875305	chr4:54990738-54990739	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs559400750	chr4:54990783-54990784	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs546678441	chr4:54990787-54990788	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs148380518	chr4:54990825-54990826	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs565675798	chr4:54990826-54990827	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs371860630	chr4:54991143-54991144	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs190296635	chr4:54991182-54991183	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs559180356	chr4:54991219-54991220	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs114591330	chr4:54991288-54991289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535555017	chr4:54991362-54991363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183093222	chr4:54991427-54991428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200071064	chr4:54991433-54991434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536922271	chr4:54991434-54991435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186762877	chr4:54991479-54991480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs6842144	chr4:54991548-54991549	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs369556109	chr4:54991551-54991552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138264760	chr4:54991587-54991588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369552824	chr4:54991913-54991914	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs560823354	chr4:54991943-54991944	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs529843350	chr4:54991960-54991961	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs146092839	chr4:54991980-54991981	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Hodgkin''s lymphoma	17606441	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
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	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
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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:249 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:54984800-54987600	Enhancers	Fetal Intestine Large	intestine
2	chr4:54985400-54987800	Enhancers	Fetal Intestine Small	intestine
3	chr4:54991200-54991600	Enhancers	H9 Cell Line	embryonic stem cell
4	chr4:55005400-55006000	Enhancers	Right Ventricle	heart
5	chr4:55005400-55006400	Enhancers	Left Ventricle	heart
6	chr4:55005600-55005800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:55005600-55006000	Enhancers	Right Atrium	heart
8	chr4:55008200-55009000	Enhancers	Thymus	Thymus
9	chr4:55008400-55009400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:55009000-55010000	Weak transcription	Thymus	Thymus
11	chr4:55010000-55011800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr4:55010000-55012400	Enhancers	Fetal Thymus	thymus
13	chr4:55010000-55012600	Enhancers	Thymus	Thymus
14	chr4:55010200-55011600	Enhancers	Primary T cells from cord blood	blood
15	chr4:55010400-55011200	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr4:55010400-55011600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr4:55010400-55012400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr4:55010400-55012600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr4:55010600-55011800	Enhancers	Primary hematopoietic stem cells	blood
20	chr4:55010800-55011400	Bivalent Enhancer	Stomach Mucosa	stomach
21	chr4:55010800-55011600	Enhancers	Dnd41	blood
22	chr4:55010800-55011600	Enhancers	HepG2	liver
23	chr4:55010800-55012400	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr4:55011000-55011600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr4:55011000-55011600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr4:55011000-55011800	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr4:55011200-55011600	Enhancers	Gastric	stomach
28	chr4:55011200-55011600	Enhancers	HSMMtube	muscle
29	chr4:55011200-55011800	Enhancers	HSMM	muscle
30	chr4:55011600-55015600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr4:55015400-55016000	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr4:55015600-55015800	Bivalent/Poised TSS	Adipose Nuclei	Adipose
33	chr4:55015600-55016000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr4:55015600-55016000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr4:55015600-55016000	Active TSS	Ovary	ovary
36	chr4:55015800-55016000	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
37	chr4:55016000-55018600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr4:55018400-55020200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:55018400-55020400	Enhancers	HMEC	breast
40	chr4:55018400-55020400	Enhancers	NHEK	skin
41	chr4:55018600-55018800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:55018600-55019600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr4:55018600-55019800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr4:55018600-55019800	Enhancers	Muscle Satellite Cultured Cells	--
45	chr4:55018600-55019800	Enhancers	NH-A	brain
46	chr4:55018600-55019800	Enhancers	NHLF	lung
47	chr4:55018600-55020000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr4:55018600-55020000	Enhancers	HSMMtube	muscle
49	chr4:55018600-55020200	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr4:55018600-55020200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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