Variant report

Variant	esv2757123
Chromosome Location	chr5:97442526-97616089
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:567)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr5:97523617-97523994	IMR90	lung:	n/a	n/a
2	CEBPB	chr5:97608471-97608702	A549	lung:	n/a	n/a
3	CEBPB	chr5:97608531-97608770	IMR90	lung:	n/a	n/a
4	CEBPB	chr5:97540112-97540365	HepG2	liver:	n/a	chr5:97540239-97540250
5	CEBPB	chr5:97597425-97597751	HepG2	liver:	n/a	chr5:97597602-97597615 chr5:97597603-97597614
6	CEBPB	chr5:97597480-97597748	IMR90	lung:	n/a	chr5:97597602-97597615 chr5:97597603-97597614
7	CEBPB	chr5:97462762-97462813	HepG2	liver:	n/a	chr5:97462789-97462800
8	CEBPB	chr5:97584522-97585081	IMR90	lung:	n/a	n/a
9	CEBPB	chr5:97445423-97446497	IMR90	lung:	n/a	chr5:97446047-97446060 chr5:97446049-97446060 chr5:97446049-97446060 chr5:97446047-97446060
10	CEBPB	chr5:97540115-97540315	A549	lung:	n/a	chr5:97540239-97540250
11	CEBPB	chr5:97584633-97584906	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr5:97523691-97523908	A549	lung:	n/a	n/a
13	CTCF	chr5:97447500-97447650	AG04450	lung:	n/a	n/a
14	CTCF	chr5:97612600-97612750	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr5:97611700-97611850	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr5:97447477-97447721	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr5:97458780-97458930	HMF	breast:	n/a	n/a
18	CTCF	chr5:97457720-97457870	GM12870	blood:	n/a	n/a
19	CTCF	chr5:97458780-97458930	AG09309	skin:	n/a	n/a
20	CTCF	chr5:97457400-97457550	HepG2	liver:	n/a	n/a
21	CTCF	chr5:97457360-97457510	HEK293	kidney:	n/a	n/a
22	CTCF	chr5:97447500-97447650	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr5:97458860-97458964	ProgFib	skin:	n/a	n/a
24	CTCF	chr5:97458760-97458910	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr5:97447520-97447670	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr5:97457360-97457510	GM12873	blood:	n/a	n/a
27	CTCF	chr5:97552500-97552650	HAc	cerebellar:	n/a	n/a
28	CTCF	chr5:97611680-97611830	AG09309	skin:	n/a	n/a
29	CTCF	chr5:97450007-97450030	GM20000	blood:	n/a	n/a
30	CTCF	chr5:97447519-97447655	MCF-7	breast:	n/a	n/a
31	CTCF	chr5:97458760-97458910	HCM	heart:	n/a	n/a
32	CTCF	chr5:97447560-97447710	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr5:97457340-97457490	GM12870	blood:	n/a	n/a
34	CTCF	chr5:97457320-97457470	GM12865	blood:	n/a	n/a
35	CTCF	chr5:97458800-97458950	HVMF	connective:	n/a	n/a
36	CTCF	chr5:97552620-97552770	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr5:97447480-97447630	AG09319	gingival:	n/a	n/a
38	CTCF	chr5:97447540-97447690	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr5:97611700-97611850	HRE	kidney:	n/a	n/a
40	CTCF	chr5:97447520-97447670	HCFaa	heart:	n/a	n/a
41	CTCF	chr5:97447520-97447670	GM12868	blood:	n/a	n/a
42	CTCF	chr5:97447520-97447670	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr5:97457380-97457530	GM12875	blood:	n/a	n/a
44	CTCF	chr5:97493220-97493370	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr5:97458800-97458950	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:97457362-97457544	GM13977	blood:	n/a	n/a
47	CTCF	chr5:97457308-97457454	K562	blood:	n/a	n/a
48	CTCF	chr5:97611720-97611870	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr5:97458720-97458870	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr5:97611720-97611870	NHEK	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:97445281-97445331	K562	blood:	n/a
2	chr5:97445281-97445331	AG09309	skin:	n/a
3	chr5:97445281-97445331	HRPEpiC	eye:	n/a
4	chr5:97445281-97445331	GM12891	blood:	n/a
5	chr5:97445281-97445331	HIPEpiC	eye:	n/a
6	chr5:97445281-97445331	AG09319	gingival:	n/a
7	chr5:97445281-97445331	PrEC	prostate:	n/a
8	chr5:97445281-97445331	GM12878	blood:	n/a
9	chr5:97445281-97445331	GM06990	blood:	n/a
10	chr5:97445281-97445331	HCM	heart:	n/a
11	chr5:97445281-97445331	NT2-D1	testis:	n/a
12	chr5:97445281-97445331	GM12892	blood:	n/a
13	chr5:97445281-97445331	PANC-1	pancreas:	n/a
14	chr5:97445281-97445331	SK-N-SH_RA	brain:	n/a
15	chr5:97445281-97445331	AG04449	skin:	fetal
16	chr5:97445281-97445331	BJ	skin:	n/a
17	chr5:97445281-97445331	HCT-116	colon:	n/a
18	chr5:97445281-97445331	Hepatocyte	liver:	n/a
19	chr5:97445281-97445331	LNCaP	prostate:	n/a
20	chr5:97445281-97445331	NH-A	brain:	n/a
21	chr5:97445281-97445331	HCPEpiC	choroid plexus:	n/a
22	chr5:97445281-97445331	ECC-1	luminal epithelium:	n/a
23	chr5:97445281-97445331	ovcar-3	ovarian:	n/a
24	chr5:97445281-97445331	IMR90	lung:	fetal
25	chr5:97445281-97445331	HRCEpiC	kidney:	n/a
26	chr5:97445281-97445331	HEEpiC	esophagus:	n/a
27	chr5:97445281-97445331	T-47D	breast:	n/a
28	chr5:97445281-97445331	MCF-7	breast:	n/a
29	chr5:97445281-97445331	HEK293	kidney:	embryo
30	chr5:97445281-97445331	HMEC	breast:	n/a
31	chr5:97445281-97445331	AoSMC	blood vessel:	n/a
32	chr5:97445281-97445331	SAEC	small airway:	n/a
33	chr5:97445281-97445331	HCF	heart:	n/a
34	chr5:97445281-97445331	NHBE	bronchial:	n/a
35	chr5:97445281-97445331	U87	brain:	n/a
36	chr5:97445281-97445331	HepG2	liver:	n/a
37	chr5:97445281-97445331	HRE	kidney:	n/a
38	chr5:97445281-97445331	MCF10A-Er-Src	breast:	n/a
39	chr5:97445281-97445331	SK-N-SH	brain:	n/a
40	chr5:97445281-97445331	HPAEpiC	pulmonary alveolar:	n/a
41	chr5:97445281-97445331	SKMC	muscle:	n/a
42	chr5:97445281-97445331	AG04450	lung:	fetal
43	chr5:97445281-97445331	Caco-2	colon:	n/a
44	chr5:97445281-97445331	A549	lung:	n/a
45	chr5:97445281-97445331	GM19239	blood:	n/a
46	chr5:97445281-97445331	SK-N-MC	brain:	n/a
47	chr5:97445281-97445331	Hela-S3	cervix:	n/a
48	chr5:97445281-97445331	HNPCEpiC	eye:	n/a
49	chr5:97445281-97445331	NB4	blood:	n/a
50	chr5:97445281-97445331	Jurkat	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:97521008..97523916-chr5:97529057..97531855,2	MCF-7	breast:
2	chr5:97546193..97548925-chr5:97549441..97552160,2	K562	blood:
3	chr5:97615949..97618290-chr5:97620124..97621957,2	MCF-7	breast:
4	chr5:97535739..97538570-chr5:97541760..97544389,2	K562	blood:
5	chr5:97521008..97523916-chr5:97529057..97531855,2	MCF-7	breast:
6	chr5:97593547..97596828-chr5:97596937..97599291,3	K562	blood:
7	chr5:97593547..97596828-chr5:97596937..97599291,3	K562	blood:
8	chr5:97535739..97538570-chr5:97541760..97544389,2	K562	blood:
9	chr5:97546193..97548925-chr5:97549441..97552160,2	K562	blood:
10	chr5:97490515..97493248-chr5:97494183..97497100,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGMB-7	chr5:97538763-97538843	NONHSAT102941
2	lnc-RGMB-7	chr5:97540456-97540897	NONHSAT102941
3	lnc-CHD1-2	chr5:97496651-97496897	XLOC_004935
4	lnc-CHD1-2	chr5:97496404-97496496	XLOC_004935
5	lnc-CHD1-2	chr5:97496010-97496123	XLOC_004935

No data

Variant related genes	Relation type
ENSG00000248901	TF binding region
ENSG00000238000	TF binding region
ENSG00000249135	TF binding region
ENSG00000248901	CpG island
ENSG00000238000	CpG island
ENSG00000249135	CpG island
ENSG00000248901	chromatin interactions
ACTR2	miRNA target sites
IKBKE	miRNA target sites
AQP1	miRNA target sites
SEC14L1	miRNA target sites

Extended variants
information (count: 6917 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:6917 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6867072	chr5:97442526-97442527	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183278729	chr5:97442559-97442560	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142193669	chr5:97442596-97442597	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577709586	chr5:97442611-97442612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201828824	chr5:97442693-97442694	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79757534	chr5:97442694-97442695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563358186	chr5:97442722-97442723	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113800742	chr5:97442723-97442724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs113533675	chr5:97442726-97442727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201774965	chr5:97442727-97442728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs56206860	chr5:97442733-97442734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200115191	chr5:97442739-97442740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199565186	chr5:97442740-97442741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542731917	chr5:97442752-97442753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547805700	chr5:97442754-97442755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115606815	chr5:97442778-97442779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187811772	chr5:97442795-97442796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78019122	chr5:97442820-97442821	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533313714	chr5:97442835-97442836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532355649	chr5:97442866-97442867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10044895	chr5:97442878-97442879	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs79901066	chr5:97442886-97442887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184719532	chr5:97442918-97442919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs59887800	chr5:97442933-97442934	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs58672630	chr5:97442940-97442941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565881915	chr5:97442987-97442988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553601949	chr5:97443011-97443012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs55760025	chr5:97443016-97443017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369027890	chr5:97443038-97443039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374585832	chr5:97443052-97443053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372898908	chr5:97443066-97443067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138480588	chr5:97443089-97443090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139884082	chr5:97443091-97443092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569877058	chr5:97443111-97443112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs56049557	chr5:97443159-97443160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79574500	chr5:97443170-97443171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143288927	chr5:97443288-97443289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs57507818	chr5:97443289-97443290	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs56069605	chr5:97443300-97443301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577279371	chr5:97443352-97443353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs578025929	chr5:97443365-97443366	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111643529	chr5:97443482-97443483	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs565792581	chr5:97443495-97443496	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs187453537	chr5:97443525-97443526	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs200226965	chr5:97443535-97443536	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs115295819	chr5:97443583-97443584	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs58094358	chr5:97443609-97443610	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs542308772	chr5:97443637-97443638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs59816694	chr5:97443642-97443643	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs192634221	chr5:97443669-97443670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
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
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	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
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21611746	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97432400-97443400	Weak transcription	NH-A	brain
2	chr5:97436200-97442600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr5:97436200-97443400	Weak transcription	HMEC	breast
4	chr5:97438800-97442800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr5:97439800-97445000	Enhancers	NHDF-Ad	bronchial
6	chr5:97440000-97443200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr5:97440200-97447800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr5:97440600-97442800	Enhancers	NHLF	lung
9	chr5:97440800-97442600	Enhancers	Adipose Nuclei	Adipose
10	chr5:97440800-97445000	Enhancers	HSMM	muscle
11	chr5:97441400-97444600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr5:97441400-97444600	Enhancers	Muscle Satellite Cultured Cells	--
13	chr5:97441800-97442600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr5:97441800-97442600	Enhancers	Fetal Lung	lung
15	chr5:97442000-97442600	Enhancers	HUVEC	blood vessel
16	chr5:97442000-97445000	Enhancers	Osteobl	bone
17	chr5:97442200-97444200	Weak transcription	HSMMtube	muscle
18	chr5:97442200-97446400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr5:97442200-97447600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr5:97442400-97442600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr5:97442400-97443600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:97442600-97442800	Enhancers	Fetal Muscle Leg	muscle
23	chr5:97442600-97443000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr5:97442600-97443000	Weak transcription	HUVEC	blood vessel
25	chr5:97442600-97444600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr5:97442600-97445000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr5:97442600-97446000	Weak transcription	Fetal Lung	lung
28	chr5:97442800-97443200	Weak transcription	NHLF	lung
29	chr5:97442800-97444000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr5:97442800-97444200	Weak transcription	Fetal Muscle Leg	muscle
31	chr5:97443000-97445000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr5:97443000-97447000	Enhancers	HUVEC	blood vessel
33	chr5:97443200-97443600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr5:97443200-97444800	Enhancers	NHEK	skin
35	chr5:97443200-97445000	Enhancers	NHLF	lung
36	chr5:97443400-97443600	Flanking Active TSS	NH-A	brain
37	chr5:97443400-97444000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr5:97443400-97447800	Enhancers	HMEC	breast
39	chr5:97443600-97443800	Enhancers	NH-A	brain
40	chr5:97443600-97444600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr5:97443600-97446000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr5:97443800-97444000	Flanking Active TSS	NH-A	brain
43	chr5:97444000-97444200	Enhancers	Fetal Stomach	stomach
44	chr5:97444000-97444400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr5:97444000-97444400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr5:97444000-97444400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr5:97444000-97444600	Enhancers	NH-A	brain
48	chr5:97444000-97444800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr5:97444200-97444400	Enhancers	Fetal Muscle Leg	muscle
50	chr5:97444200-97444400	Enhancers	HSMMtube	muscle

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