Variant report

Variant	nsv1022981
Chromosome Location	chr5:120583543-120691755
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	chr5:120609660-120610180	A549	lung:	n/a	n/a
3	ATF3	chr5:120609671-120610135	A549	lung:	n/a	n/a
4	ATF3	chr5:120587704-120588047	A549	lung:	n/a	n/a
5	BACH1	chr5:120609897-120610216	K562	blood:	n/a	n/a
6	BCL3	chr5:120587530-120588099	A549	lung:	n/a	n/a
7	BCL3	chr5:120609574-120610233	A549	lung:	n/a	n/a
8	BCL3	chr5:120609611-120610175	A549	lung:	n/a	n/a
9	CBX3	chr5:120587730-120588017	HCT-116	colon:	n/a	n/a
10	CBX3	chr5:120609626-120610276	HCT-116	colon:	n/a	n/a
11	CEBPB	chr5:120587556-120588192	A549	lung:	n/a	n/a
12	CEBPB	chr5:120587688-120588575	A549	lung:	n/a	n/a
13	CEBPB	chr5:120609529-120610117	A549	lung:	n/a	chr5:120609623-120609636
14	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
15	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
16	CEBPB	chr5:120628443-120628634	K562	blood:	n/a	chr5:120628524-120628535
17	CEBPB	chr5:120665080-120665327	A549	lung:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
18	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
19	CEBPB	chr5:120665091-120665434	K562	blood:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
20	CEBPB	chr5:120650741-120651097	A549	lung:	n/a	n/a
21	CEBPB	chr5:120665178-120665393	Hela-S3	cervix:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
22	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
23	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
24	CEBPB	chr5:120665137-120665399	H1-hESC	embryonic stem cell:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
25	CEBPB	chr5:120609521-120610150	IMR90	lung:	n/a	chr5:120609623-120609636
26	CEBPB	chr5:120650781-120651061	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:120602594-120602886	K562	blood:	n/a	chr5:120602751-120602762
28	CEBPB	chr5:120587635-120588242	HCT-116	colon:	n/a	n/a
29	CEBPB	chr5:120650883-120651016	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr5:120609534-120610174	Hela-S3	cervix:	n/a	chr5:120609623-120609636
31	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
32	CEBPB	chr5:120602603-120602824	HepG2	liver:	n/a	chr5:120602751-120602762
33	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
34	CEBPB	chr5:120615503-120615753	K562	blood:	n/a	n/a
35	CEBPB	chr5:120587649-120588101	HCT-116	colon:	n/a	n/a
36	CEBPB	chr5:120650749-120651103	K562	blood:	n/a	n/a
37	CEBPB	chr5:120587647-120588158	A549	lung:	n/a	n/a
38	CEBPB	chr5:120609455-120610277	A549	lung:	n/a	chr5:120609623-120609636
39	CEBPB	chr5:120665120-120665392	HepG2	liver:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
40	CEBPB	chr5:120650738-120651081	IMR90	lung:	n/a	n/a
41	CEBPB	chr5:120587696-120588057	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr5:120650738-120651104	HepG2	liver:	n/a	n/a
43	CEBPB	chr5:120615541-120615802	K562	blood:	n/a	n/a
44	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
45	CEBPB	chr5:120602581-120602901	IMR90	lung:	n/a	chr5:120602751-120602762
46	CEBPB	chr5:120672127-120672318	H1-hESC	embryonic stem cell:	n/a	n/a
47	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
48	CEBPB	chr5:120665093-120665414	IMR90	lung:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
49	CEBPB	chr5:120602604-120602822	A549	lung:	n/a	chr5:120602751-120602762
50	CEBPD	chr5:120615370-120615697	K562	blood:	n/a	n/a

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

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

Variant related genes	Relation type
ENSG00000229855	TF binding region

Extended variants
information (count: 2202 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2202 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142236957	chr5:120583621-120583622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs78226997	chr5:120583640-120583641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540975743	chr5:120583647-120583648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546667611	chr5:120583680-120583681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138968506	chr5:120583726-120583727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190842003	chr5:120583753-120583754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs200366229	chr5:120583766-120583767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576959879	chr5:120583867-120583868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182988855	chr5:120583877-120583878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551213941	chr5:120583888-120583889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569196675	chr5:120583895-120583896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370520768	chr5:120583901-120583902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375684659	chr5:120583919-120583920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111284809	chr5:120583935-120583936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188656405	chr5:120583970-120583971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142185589	chr5:120584047-120584048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371444352	chr5:120584052-120584053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs551543178	chr5:120584072-120584073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541193512	chr5:120584100-120584101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs200646790	chr5:120584101-120584102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146363633	chr5:120584148-120584149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540415780	chr5:120584169-120584170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558985075	chr5:120584187-120584188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192787510	chr5:120584199-120584200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs200227363	chr5:120584200-120584201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187012970	chr5:120586023-120586024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527493934	chr5:120586053-120586054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191889504	chr5:120586062-120586063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2914062	chr5:120586075-120586076	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs531469095	chr5:120586107-120586108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs117925655	chr5:120586153-120586154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568073322	chr5:120586172-120586173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs138393602	chr5:120586251-120586252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373643134	chr5:120586275-120586276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183322312	chr5:120586282-120586283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566289812	chr5:120586303-120586304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142011057	chr5:120586334-120586335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150683050	chr5:120586371-120586372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188396674	chr5:120586392-120586393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557132910	chr5:120586419-120586420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537692086	chr5:120586433-120586434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191699013	chr5:120586445-120586446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553868438	chr5:120586453-120586454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182477062	chr5:120586465-120586466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186754735	chr5:120586495-120586496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572240547	chr5:120586585-120586586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545696460	chr5:120586588-120586589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542718545	chr5:120586589-120586590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76244659	chr5:120586665-120586666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs3991032	chr5:120586669-120586670	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	chr5:120580800-120584200	Enhancers	Dnd41	blood
2	chr5:120586000-120587400	Weak transcription	A549	lung
3	chr5:120586800-120588800	Enhancers	HUVEC	blood vessel
4	chr5:120587400-120587600	Enhancers	A549	lung
5	chr5:120587400-120587800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr5:120587600-120588000	Active TSS	A549	lung
7	chr5:120587600-120588400	Enhancers	Muscle Satellite Cultured Cells	--
8	chr5:120587800-120588200	Enhancers	Osteobl	bone
9	chr5:120587800-120588400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr5:120588000-120588400	Flanking Active TSS	A549	lung
11	chr5:120588200-120588800	Enhancers	HMEC	breast
12	chr5:120588400-120589000	Enhancers	A549	lung
13	chr5:120588800-120593400	Weak transcription	HUVEC	blood vessel
14	chr5:120593000-120594000	Enhancers	Dnd41	blood
15	chr5:120593200-120593600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr5:120593400-120593800	Enhancers	HUVEC	blood vessel
17	chr5:120598600-120598800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr5:120598600-120598800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr5:120598800-120599400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr5:120599000-120599200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr5:120600600-120600800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr5:120600600-120601400	Enhancers	A549	lung
23	chr5:120600600-120602000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr5:120600800-120609600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr5:120601400-120609200	Weak transcription	A549	lung
26	chr5:120609200-120609600	Enhancers	A549	lung
27	chr5:120609200-120609800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr5:120609400-120609600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr5:120609400-120609600	Enhancers	Muscle Satellite Cultured Cells	--
30	chr5:120609400-120609600	Enhancers	NHDF-Ad	bronchial
31	chr5:120609400-120609800	Enhancers	Osteobl	bone
32	chr5:120609600-120609800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
33	chr5:120609600-120610000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr5:120609600-120610000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr5:120609600-120610000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr5:120609600-120610000	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr5:120609600-120610000	Flanking Active TSS	NHDF-Ad	bronchial
38	chr5:120609600-120610200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr5:120609600-120610200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr5:120609600-120610200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr5:120609600-120610200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr5:120609600-120610200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr5:120609600-120610200	Flanking Active TSS	A549	lung
44	chr5:120609600-120610200	Enhancers	Dnd41	blood
45	chr5:120609600-120610200	Enhancers	K562	blood
46	chr5:120609600-120610200	Enhancers	NHLF	lung
47	chr5:120609600-120610400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr5:120609600-120610400	Enhancers	Hela-S3	cervix
49	chr5:120609600-120610400	Enhancers	HMEC	breast
50	chr5:120609600-120610400	Enhancers	NH-A	brain

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