Variant report

Variant	nsv518883
Chromosome Location	chr5:120591425-120708748
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	ATF1	chr5:120609797-120610099	K562	blood:	n/a	n/a
2	ATF3	chr5:120609671-120610135	A549	lung:	n/a	n/a
3	ATF3	chr5:120609660-120610180	A549	lung:	n/a	n/a
4	BACH1	chr5:120609897-120610216	K562	blood:	n/a	n/a
5	BCL3	chr5:120609611-120610175	A549	lung:	n/a	n/a
6	BCL3	chr5:120609574-120610233	A549	lung:	n/a	n/a
7	BRCA1	chr5:120694893-120694952	GM12878	blood:	n/a	n/a
8	CBX3	chr5:120609626-120610276	HCT-116	colon:	n/a	n/a
9	CEBPB	chr5:120609521-120610150	IMR90	lung:	n/a	chr5:120609623-120609636
10	CEBPB	chr5:120640581-120640927	A549	lung:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
11	CEBPB	chr5:120640568-120640898	H1-hESC	embryonic stem cell:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
12	CEBPB	chr5:120640554-120640918	ECC-1	luminal epithelium:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
13	CEBPB	chr5:120650738-120651081	IMR90	lung:	n/a	n/a
14	CEBPB	chr5:120665080-120665327	A549	lung:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
15	CEBPB	chr5:120609455-120610277	A549	lung:	n/a	chr5:120609623-120609636
16	CEBPB	chr5:120650738-120651104	HepG2	liver:	n/a	n/a
17	CEBPB	chr5:120702194-120702588	IMR90	lung:	n/a	n/a
18	CEBPB	chr5:120602604-120602822	A549	lung:	n/a	chr5:120602751-120602762
19	CEBPB	chr5:120640550-120640906	HepG2	liver:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
20	CEBPB	chr5:120650781-120651061	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr5:120640581-120640914	A549	lung:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
22	CEBPB	chr5:120609534-120610174	Hela-S3	cervix:	n/a	chr5:120609623-120609636
23	CEBPB	chr5:120672127-120672318	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr5:120640558-120640915	IMR90	lung:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
25	CEBPB	chr5:120665120-120665392	HepG2	liver:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
26	CEBPB	chr5:120665093-120665414	IMR90	lung:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
27	CEBPB	chr5:120702142-120702659	A549	lung:	n/a	n/a
28	CEBPB	chr5:120609529-120610117	A549	lung:	n/a	chr5:120609623-120609636
29	CEBPB	chr5:120602594-120602886	K562	blood:	n/a	chr5:120602751-120602762
30	CEBPB	chr5:120640491-120640969	A549	lung:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
31	CEBPB	chr5:120694614-120695283	A549	lung:	n/a	n/a
32	CEBPB	chr5:120615541-120615802	K562	blood:	n/a	n/a
33	CEBPB	chr5:120650883-120651016	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr5:120702168-120702578	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr5:120665137-120665399	H1-hESC	embryonic stem cell:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
36	CEBPB	chr5:120665178-120665393	Hela-S3	cervix:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
37	CEBPB	chr5:120628443-120628634	K562	blood:	n/a	chr5:120628524-120628535
38	CEBPB	chr5:120640581-120640912	Hela-S3	cervix:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
39	CEBPB	chr5:120602603-120602824	HepG2	liver:	n/a	chr5:120602751-120602762
40	CEBPB	chr5:120650749-120651103	K562	blood:	n/a	n/a
41	CEBPB	chr5:120665091-120665434	K562	blood:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
42	CEBPB	chr5:120615503-120615753	K562	blood:	n/a	n/a
43	CEBPB	chr5:120650741-120651097	A549	lung:	n/a	n/a
44	CEBPB	chr5:120602581-120602901	IMR90	lung:	n/a	chr5:120602751-120602762
45	CEBPB	chr5:120640541-120640899	K562	blood:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
46	CEBPB	chr5:120694786-120695190	A549	lung:	n/a	n/a
47	CEBPD	chr5:120615370-120615697	K562	blood:	n/a	n/a
48	CHD2	chr5:120609726-120610137	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr5:120669952-120670015	GM10266	blood:	n/a	n/a
50	CTCF	chr5:120618420-120618570	GM12866	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:120631738..120633506-chr5:120633517..120635841,2	K562	blood:
2	chr5:120621053..120623969-chr5:120627723..120630035,2	MCF-7	breast:
3	chr5:120604790..120607005-chr5:120607199..120609992,2	K562	blood:
4	chr5:120684041..120685887-chr5:120689318..120691883,2	K562	blood:
5	chr5:120643239..120645271-chr5:120645522..120647194,2	K562	blood:
6	chr5:120597959..120600237-chr5:120894989..120897698,2	K562	blood:
7	chr5:120628569..120631260-chr5:120631938..120634860,2	MCF-7	breast:
8	chr5:120643239..120645271-chr5:120645522..120647194,2	K562	blood:
9	chr5:120631738..120633506-chr5:120633517..120635841,2	K562	blood:
10	chr5:120628569..120631260-chr5:120631938..120634860,2	MCF-7	breast:
11	chr5:120604790..120607005-chr5:120607199..120609992,2	K562	blood:
12	chr5:120684041..120685887-chr5:120689318..120691883,2	K562	blood:
13	chr5:120621053..120623969-chr5:120627723..120630035,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FTMT-2	chr5:120685681-120686145	ENSG00000229855.4
2	lnc-FTMT-2	chr5:120659736-120659765	ENSG00000229855.4
3	lnc-FTMT-3	chr5:120698697-120701009	NONHSAT103459
4	lnc-FTMT-2	chr5:120656659-120656681	NONHSAT103454
5	lnc-FTMT-2	chr5:120661117-120661532	XLOC_004529
6	lnc-FTMT-2	chr5:120656575-120656681	ENSG00000229855.4
7	lnc-FTMT-2	chr5:120683388-120683561	ENSG00000229855.4
8	lnc-FTMT-2	chr5:120658245-120658302	ENSG00000229855.4
9	lnc-FTMT-2	chr5:120656575-120656681	ENSG00000229855.4
10	lnc-FTMT-2	chr5:120692501-120693093	ENSG00000229855.4
11	lnc-FTMT-2	chr5:120658244-120658302	NONHSAT103454
12	lnc-FTMT-2	chr5:120658249-120658302	ENSG00000229855.4
13	lnc-FTMT-2	chr5:120659733-120659765	NONHSAT103454
14	lnc-FTMT-2	chr5:120658249-120658302	ENSG00000229855.4
15	lnc-FTMT-2	chr5:120661122-120661174	ENSG00000229855.4
16	lnc-FTMT-2	chr5:120658245-120658302	XLOC_004529
17	lnc-FTMT-2	chr5:120649656-120649899	ENSG00000229855.4
18	lnc-FTMT-2	chr5:120661041-120661595	NONHSAT103454
19	lnc-FTMT-2	chr5:120661117-120661651	ENSG00000229855.4
20	lnc-FTMT-2	chr5:120621476-120621568	ENSG00000229855.4
21	lnc-FTMT-2	chr5:120659736-120659765	ENSG00000229855.4
22	lnc-FTMT-2	chr5:120658249-120658302	ENSG00000229855.4
23	lnc-FTMT-2	chr5:120661117-120661793	ENSG00000229855.4
24	lnc-FTMT-2	chr5:120659736-120659765	XLOC_004529
25	lnc-FTMT-2	chr5:120683388-120683561	ENSG00000229855.4
26	lnc-FTMT-2	chr5:120649672-120649899	ENSG00000229855.4
27	lnc-FTMT-2	chr5:120661117-120661175	ENSG00000229855.4

Variant related genes	Relation type
ENSG00000229855	TF binding region

Extended variants
information (count: 2310 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2310 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386691784	chr5:120591425-120591426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs114241170	chr5:120591426-120591427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568667822	chr5:120591447-120591448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535657284	chr5:120591513-120591514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs368097371	chr5:120591523-120591524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566244804	chr5:120591529-120591530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540098224	chr5:120591541-120591542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558626144	chr5:120591558-120591559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138303612	chr5:120591606-120591607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs13183288	chr5:120591635-120591636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556275831	chr5:120591638-120591639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554711423	chr5:120591661-120591662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574437978	chr5:120591671-120591672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs143876055	chr5:120591687-120591688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560249105	chr5:120591688-120591689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371601126	chr5:120591790-120591791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545686460	chr5:120591799-120591800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564189699	chr5:120591800-120591801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181504242	chr5:120591823-120591824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549897020	chr5:120591866-120591867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185756697	chr5:120591881-120591882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201812071	chr5:120591923-120591924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75508483	chr5:120591933-120591934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs397999118	chr5:120591934-120591935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529339929	chr5:120591984-120591985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576151897	chr5:120592035-120592036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190176364	chr5:120592073-120592074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549299302	chr5:120592093-120592094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35609040	chr5:120592102-120592103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111848902	chr5:120592116-120592117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10040125	chr5:120592185-120592186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs552078594	chr5:120592199-120592200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201167007	chr5:120592276-120592277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182970641	chr5:120592298-120592299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187591166	chr5:120592320-120592321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192485098	chr5:120592339-120592340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183931147	chr5:120592391-120592392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553728115	chr5:120592420-120592421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187550289	chr5:120592456-120592457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192188141	chr5:120592468-120592469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148331970	chr5:120592477-120592478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543413691	chr5:120592488-120592489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141459684	chr5:120592517-120592518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529408261	chr5:120592538-120592539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184224657	chr5:120592599-120592600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150777650	chr5:120592600-120592601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187151266	chr5:120592638-120592639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192694786	chr5:120592704-120592705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570383530	chr5:120592706-120592707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139122676	chr5:120592707-120592708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:120588800-120593400	Weak transcription	HUVEC	blood vessel
2	chr5:120593000-120594000	Enhancers	Dnd41	blood
3	chr5:120593200-120593600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr5:120593400-120593800	Enhancers	HUVEC	blood vessel
5	chr5:120598600-120598800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr5:120598600-120598800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr5:120598800-120599400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:120599000-120599200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr5:120600600-120600800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr5:120600600-120601400	Enhancers	A549	lung
11	chr5:120600600-120602000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr5:120600800-120609600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr5:120601400-120609200	Weak transcription	A549	lung
14	chr5:120609200-120609600	Enhancers	A549	lung
15	chr5:120609200-120609800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr5:120609400-120609600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr5:120609400-120609600	Enhancers	Muscle Satellite Cultured Cells	--
18	chr5:120609400-120609600	Enhancers	NHDF-Ad	bronchial
19	chr5:120609400-120609800	Enhancers	Osteobl	bone
20	chr5:120609600-120609800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
21	chr5:120609600-120610000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr5:120609600-120610000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr5:120609600-120610000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr5:120609600-120610000	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr5:120609600-120610000	Flanking Active TSS	NHDF-Ad	bronchial
26	chr5:120609600-120610200	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr5:120609600-120610200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr5:120609600-120610200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr5:120609600-120610200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr5:120609600-120610200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr5:120609600-120610200	Flanking Active TSS	A549	lung
32	chr5:120609600-120610200	Enhancers	Dnd41	blood
33	chr5:120609600-120610200	Enhancers	K562	blood
34	chr5:120609600-120610200	Enhancers	NHLF	lung
35	chr5:120609600-120610400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr5:120609600-120610400	Enhancers	Hela-S3	cervix
37	chr5:120609600-120610400	Enhancers	HMEC	breast
38	chr5:120609600-120610400	Enhancers	NH-A	brain
39	chr5:120609600-120610600	Enhancers	HUVEC	blood vessel
40	chr5:120609800-120610000	Enhancers	Muscle Satellite Cultured Cells	--
41	chr5:120609800-120610200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:120609800-120610200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr5:120609800-120610200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr5:120609800-120610200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr5:120609800-120610200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr5:120609800-120610200	Flanking Active TSS	Osteobl	bone
47	chr5:120610000-120610200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr5:120610000-120610200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr5:120610000-120610200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
50	chr5:120610000-120610400	Enhancers	NHDF-Ad	bronchial

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