Variant report

Variant	nsv598289
Chromosome Location	chr5:59714130-59757242
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:202)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:202 , 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	chr5:59722961-59722993	K562	blood:	n/a	n/a
2	ARID3A	chr5:59712885-59714270	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:59742744-59743990	HepG2	liver:	n/a	chr5:59743535-59743551
4	BHLHE40	chr5:59742844-59743730	HepG2	liver:	n/a	n/a
5	BHLHE40	chr5:59743262-59743636	HepG2	liver:	n/a	n/a
6	BHLHE40	chr5:59743228-59743638	HepG2	liver:	n/a	n/a
7	CCNT2	chr5:59747083-59747168	K562	blood:	n/a	n/a
8	CEBPB	chr5:59740891-59741112	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr5:59738481-59738678	HepG2	liver:	n/a	chr5:59738605-59738616
10	CEBPB	chr5:59744195-59744769	A549	lung:	n/a	chr5:59744753-59744765
11	CEBPB	chr5:59744444-59744829	Hela-S3	cervix:	n/a	chr5:59744753-59744765
12	CTCF	chr5:59754583-59754809	MCF-7	breast:	n/a	n/a
13	CTCF	chr5:59742740-59742890	HepG2	liver:	n/a	n/a
14	CTCF	chr5:59754620-59754770	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr5:59754600-59754750	A549	lung:	n/a	n/a
16	CTCF	chr5:59754580-59754730	AG09309	skin:	n/a	n/a
17	CTCF	chr5:59754600-59754750	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr5:59754640-59754790	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr5:59732400-59732550	GM12875	blood:	n/a	n/a
20	CTCF	chr5:59754111-59754159	Fibrobl	skin:	n/a	n/a
21	CTCF	chr5:59755768-59755822	Lung_OC	lung:	n/a	n/a
22	CTCF	chr5:59732460-59732610	RPTEC	kidney:	n/a	n/a
23	CTCF	chr5:59754649-59754762	HepG2	liver:	n/a	n/a
24	CTCF	chr5:59754580-59754730	HepG2	liver:	n/a	n/a
25	CTCF	chr5:59754590-59754775	HepG2	liver:	n/a	n/a
26	CTCF	chr5:59732400-59732550	GM12873	blood:	n/a	n/a
27	CTCF	chr5:59754620-59754770	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr5:59754620-59754770	HAc	cerebellar:	n/a	n/a
29	CTCF	chr5:59732460-59732610	GM12878	blood:	n/a	n/a
30	CTCF	chr5:59754609-59754797	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr5:59732490-59732534	GM12878	blood:	n/a	n/a
32	CTCF	chr5:59754618-59754772	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr5:59732480-59732630	GM12864	blood:	n/a	n/a
34	CTCF	chr5:59754620-59754770	Caco-2	colon:	n/a	n/a
35	CTCF	chr5:59754560-59754710	GM12874	blood:	n/a	n/a
36	CTCF	chr5:59754660-59754810	BE2_C	brain:	n/a	n/a
37	CTCF	chr5:59732480-59732630	GM12873	blood:	n/a	n/a
38	CTCF	chr5:59732540-59732690	HEK293	kidney:	n/a	n/a
39	CTCF	chr5:59754600-59754750	K562	blood:	n/a	n/a
40	CTCF	chr5:59732520-59732670	GM12871	blood:	n/a	n/a
41	CTCF	chr5:59732460-59732610	GM12865	blood:	n/a	n/a
42	CTCF	chr5:59754601-59754828	K562	blood:	n/a	n/a
43	CTCF	chr5:59732460-59732610	GM12871	blood:	n/a	n/a
44	CTCF	chr5:59754610-59754792	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:59742760-59743050	HepG2	liver:	n/a	n/a
46	CTCF	chr5:59754600-59754750	SAEC	small airway:	n/a	n/a
47	CTCF	chr5:59737560-59737622	GM13976	blood:	n/a	n/a
48	CTCF	chr5:59754643-59754772	K562	blood:	n/a	n/a
49	CTCF	chr5:59754497-59754924	MCF-7	breast:	n/a	n/a
50	CTCF	chr5:59755354-59755397	Medullo	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:59727726-59727776	Hela-S3	cervix:	n/a
2	chr5:59727726-59727776	SAEC	small airway:	n/a
3	chr5:59727726-59727776	LNCaP	prostate:	n/a
4	chr5:59727726-59727776	CMK	blood:	n/a
5	chr5:59727726-59727776	HEEpiC	esophagus:	n/a
6	chr5:59727726-59727776	ProgFib	skin:	n/a
7	chr5:59727726-59727776	IMR90	lung:	fetal
8	chr5:59727726-59727776	BJ	skin:	n/a
9	chr5:59727726-59727776	K562	blood:	n/a
10	chr5:59727726-59727776	AG09309	skin:	n/a
11	chr5:59727726-59727776	GM12878	blood:	n/a
12	chr5:59727726-59727776	PANC-1	pancreas:	n/a
13	chr5:59727726-59727776	SK-N-SH_RA	brain:	n/a
14	chr5:59727726-59727776	Caco-2	colon:	n/a
15	chr5:59727726-59727776	HL-60	blood:	n/a
16	chr5:59727726-59727776	GM12891	blood:	n/a
17	chr5:59727726-59727776	HRE	kidney:	n/a
18	chr5:59727726-59727776	BE2_C	brain:	n/a
19	chr5:59727726-59727776	HMEC	breast:	n/a
20	chr5:59727726-59727776	HCPEpiC	choroid plexus:	n/a
21	chr5:59727726-59727776	AG04449	skin:	fetal
22	chr5:59727726-59727776	SK-N-MC	brain:	n/a
23	chr5:59727726-59727776	AG04450	lung:	fetal
24	chr5:59727726-59727776	NH-A	brain:	n/a
25	chr5:59727726-59727776	GM12892	blood:	n/a
26	chr5:59727726-59727776	HepG2	liver:	n/a
27	chr5:59727726-59727776	PFSK-1	brain:	n/a
28	chr5:59727726-59727776	HPAEpiC	pulmonary alveolar:	n/a
29	chr5:59727726-59727776	RPTEC	kidney:	n/a
30	chr5:59727726-59727776	HNPCEpiC	eye:	n/a
31	chr5:59727726-59727776	T-47D	breast:	n/a
32	chr5:59727726-59727776	HUVEC	blood vessel:	n/a
33	chr5:59727726-59727776	SK-N-SH	brain:	n/a
34	chr5:59727726-59727776	AG09319	gingival:	n/a
35	chr5:59727726-59727776	AoSMC	blood vessel:	n/a
36	chr5:59727726-59727776	GM06990	blood:	n/a
37	chr5:59727726-59727776	Jurkat	blood:	n/a
38	chr5:59727726-59727776	ECC-1	luminal epithelium:	n/a
39	chr5:59727726-59727776	MCF10A-Er-Src	breast:	n/a
40	chr5:59727726-59727776	MCF-7	breast:	n/a
41	chr5:59727726-59727776	HRCEpiC	kidney:	n/a
42	chr5:59727726-59727776	NHDF-neo	bronchial:	n/a
43	chr5:59727726-59727776	HCT-116	colon:	n/a
44	chr5:59727726-59727776	U87	brain:	n/a
45	chr5:59727726-59727776	H1-hESC	embryonic stem cell:	embryo
46	chr5:59727726-59727776	AG10803	skin:	n/a
47	chr5:59727726-59727776	GM19239	blood:	n/a
48	chr5:59727726-59727776	HEK293	kidney:	embryo
49	chr5:59727726-59727776	HCM	heart:	n/a
50	chr5:59727726-59727776	HIPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:59750546..59752966-chr5:59754525..59756849,2	K562	blood:
2	chr5:59700212..59701783-chr5:59712786..59715237,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000213896	TF binding region
ENSG00000224838	TF binding region
SETP21	TF binding region
PDE4D	TF binding region
ENSG00000213896	CpG island
ENSG00000224838	CpG island
SETP21	CpG island
PDE4D	CpG island
ENSG00000214244	chromatin interactions

Extended variants
information (count: 1659 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1659 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs37708	chr5:59714130-59714131	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs6868537	chr5:59714136-59714137	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs145919937	chr5:59714173-59714174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571404890	chr5:59714188-59714189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs377137508	chr5:59714232-59714233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558396726	chr5:59714255-59714256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547322727	chr5:59714258-59714259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78890595	chr5:59714271-59714272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs201826466	chr5:59714273-59714274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576529762	chr5:59714302-59714303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs142623361	chr5:59714303-59714304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556074507	chr5:59714308-59714309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs146622741	chr5:59714322-59714323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs150589160	chr5:59714335-59714336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538493936	chr5:59714342-59714343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559817424	chr5:59714368-59714369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565616752	chr5:59714432-59714433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558618657	chr5:59714438-59714439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs572465462	chr5:59714459-59714460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs34647979	chr5:59714481-59714482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541172840	chr5:59714506-59714507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189727930	chr5:59714522-59714523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574771364	chr5:59714545-59714546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183414254	chr5:59714550-59714551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187716744	chr5:59714611-59714612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192159413	chr5:59714617-59714618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546378275	chr5:59714626-59714627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113894984	chr5:59714703-59714704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559694270	chr5:59714707-59714708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562236577	chr5:59714733-59714734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185457826	chr5:59714736-59714737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547190686	chr5:59714766-59714767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369512944	chr5:59714800-59714801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567239354	chr5:59714817-59714818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs37707	chr5:59714839-59714840	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs191851568	chr5:59714847-59714848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549663099	chr5:59714849-59714850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs58224215	chr5:59714851-59714852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188320210	chr5:59714856-59714857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192974121	chr5:59714858-59714859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs184644223	chr5:59714870-59714871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs143282609	chr5:59714874-59714875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs377720367	chr5:59714889-59714890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs138570028	chr5:59714952-59714953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs554791891	chr5:59714969-59714970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs373159230	chr5:59714980-59714981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs574771537	chr5:59714996-59714997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374733429	chr5:59715034-59715035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs189519955	chr5:59715163-59715164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs180703487	chr5:59715169-59715170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	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
Hepatocellular carcinoma	16750200	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
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59712400-59716800	Enhancers	HepG2	liver
2	chr5:59713200-59716000	Weak transcription	Primary B cells from cord blood	blood
3	chr5:59716000-59716600	ZNF genes & repeats	Primary B cells from cord blood	blood
4	chr5:59716400-59716800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr5:59716400-59716800	ZNF genes & repeats	Pancreas	Pancrea
6	chr5:59716800-59717000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:59717000-59730000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr5:59727200-59766600	Weak transcription	Primary B cells from cord blood	blood
9	chr5:59730000-59730400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr5:59730400-59731000	Enhancers	Colon Smooth Muscle	Colon
11	chr5:59730400-59731800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr5:59730400-59733200	Enhancers	HepG2	liver
13	chr5:59731800-59732000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr5:59732000-59732400	Enhancers	GM12878-XiMat	blood
15	chr5:59732400-59733000	Enhancers	Primary B cells from peripheral blood	blood
16	chr5:59732400-59733400	Flanking Active TSS	GM12878-XiMat	blood
17	chr5:59732800-59733000	Enhancers	Aorta	Aorta
18	chr5:59733000-59742600	Weak transcription	Aorta	Aorta
19	chr5:59733200-59738800	Weak transcription	HepG2	liver
20	chr5:59733400-59733800	Enhancers	GM12878-XiMat	blood
21	chr5:59734000-59734400	Enhancers	Fetal Kidney	kidney
22	chr5:59738800-59742800	Enhancers	HepG2	liver
23	chr5:59740000-59741200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr5:59740000-59741600	Enhancers	Fetal Brain Male	brain
25	chr5:59740200-59740600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr5:59740400-59741000	Enhancers	Fetal Brain Female	brain
27	chr5:59740400-59741000	Enhancers	Hela-S3	cervix
28	chr5:59740600-59740800	Enhancers	Gastric	stomach
29	chr5:59741000-59744200	Weak transcription	Hela-S3	cervix
30	chr5:59741200-59741600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr5:59741600-59741800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr5:59741600-59743200	Enhancers	Stomach Mucosa	stomach
33	chr5:59741600-59744800	Weak transcription	Fetal Brain Male	brain
34	chr5:59741800-59783200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr5:59742600-59743000	Enhancers	Aorta	Aorta
36	chr5:59742600-59743000	Enhancers	A549	lung
37	chr5:59742600-59744400	Enhancers	Gastric	stomach
38	chr5:59742800-59743200	Flanking Active TSS	HepG2	liver
39	chr5:59743000-59743600	Flanking Active TSS	A549	lung
40	chr5:59743000-59743800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:59743200-59744400	Weak transcription	Stomach Mucosa	stomach
42	chr5:59743200-59745200	Enhancers	HepG2	liver
43	chr5:59743400-59743800	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr5:59743600-59744000	Active TSS	A549	lung
45	chr5:59743800-59747600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr5:59744000-59744200	Enhancers	A549	lung
47	chr5:59744200-59744400	Flanking Active TSS	A549	lung
48	chr5:59744200-59744600	Enhancers	Brain Angular Gyrus	brain
49	chr5:59744200-59744600	Active TSS	Hela-S3	cervix
50	chr5:59744400-59744600	Enhancers	Stomach Mucosa	stomach

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