Variant report

Variant	esv1797587
Chromosome Location	chr5:127156760-127196066
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	BATF	chr5:127175281-127175449	GM12878	blood:	n/a	n/a
2	BATF	chr5:127175254-127175475	GM12878	blood:	n/a	n/a
3	BCL11A	chr5:127175773-127176141	GM12878	blood:	n/a	n/a
4	BCL11A	chr5:127175260-127175446	GM12878	blood:	n/a	n/a
5	BCL11A	chr5:127175268-127175454	GM12878	blood:	n/a	n/a
6	BHLHE40	chr5:127175898-127176226	GM12878	blood:	n/a	n/a
7	BHLHE40	chr5:127175269-127175373	GM12878	blood:	n/a	n/a
8	CEBPB	chr5:127170365-127170691	Hela-S3	cervix:	n/a	chr5:127170512-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170513-127170524 chr5:127170512-127170525 chr5:127170514-127170523
9	CEBPB	chr5:127182668-127182952	A549	lung:	n/a	chr5:127182810-127182823 chr5:127182812-127182823
10	CEBPB	chr5:127170289-127170651	A549	lung:	n/a	chr5:127170512-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170513-127170524 chr5:127170512-127170525 chr5:127170514-127170523
11	CEBPB	chr5:127170331-127170703	IMR90	lung:	n/a	chr5:127170512-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170513-127170524 chr5:127170512-127170525 chr5:127170514-127170523
12	CEBPB	chr5:127170331-127170692	K562	blood:	n/a	chr5:127170512-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170513-127170524 chr5:127170512-127170525 chr5:127170514-127170523
13	CEBPB	chr5:127170205-127170819	A549	lung:	n/a	chr5:127170512-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170513-127170524 chr5:127170512-127170525 chr5:127170514-127170523
14	CEBPB	chr5:127192196-127192271	IMR90	lung:	n/a	n/a
15	CEBPB	chr5:127170335-127170700	HepG2	liver:	n/a	chr5:127170512-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170513-127170524 chr5:127170512-127170525 chr5:127170514-127170523
16	CEBPB	chr5:127159929-127160091	A549	lung:	n/a	chr5:127160002-127160013
17	CEBPB	chr5:127170377-127170632	K562	blood:	n/a	chr5:127170512-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170513-127170524 chr5:127170512-127170525 chr5:127170514-127170523
18	CEBPB	chr5:127156707-127156994	A549	lung:	n/a	n/a
19	CEBPB	chr5:127183976-127184113	HepG2	liver:	n/a	chr5:127184008-127184021 chr5:127184010-127184021 chr5:127184010-127184021 chr5:127184008-127184019
20	CEBPB	chr5:127170321-127170693	A549	lung:	n/a	chr5:127170512-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170513-127170524 chr5:127170512-127170525 chr5:127170514-127170523
21	CEBPB	chr5:127165922-127166265	IMR90	lung:	n/a	n/a
22	CEBPB	chr5:127159903-127160095	HepG2	liver:	n/a	chr5:127160002-127160013
23	CEBPB	chr5:127170359-127170662	H1-hESC	embryonic stem cell:	n/a	chr5:127170512-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170514-127170523 chr5:127170513-127170524 chr5:127170512-127170525 chr5:127170514-127170523
24	CEBPB	chr5:127159975-127160127	H1-hESC	embryonic stem cell:	n/a	chr5:127160002-127160013
25	CEBPB	chr5:127166665-127166677	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr5:127180431-127180584	MCF-7	breast:	n/a	n/a
27	CTCF	chr5:127180367-127180428	GM19239	blood:	n/a	n/a
28	CTCF	chr5:127180400-127180550	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr5:127169760-127169910	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr5:127180531-127180563	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr5:127169720-127169870	AG09319	gingival:	n/a	n/a
32	CTCF	chr5:127169786-127169969	Medullo	brain:	n/a	n/a
33	CTCF	chr5:127169800-127169950	BJ	skin:	n/a	n/a
34	CTCF	chr5:127169700-127169850	GM12865	blood:	n/a	n/a
35	CTCF	chr5:127169680-127169950	A549	lung:	n/a	n/a
36	CTCF	chr5:127169836-127169857	GM13977	blood:	n/a	n/a
37	CTCF	chr5:127169740-127169890	NHEK	skin:	n/a	n/a
38	CTCF	chr5:127169776-127169944	LNCaP	prostate:	n/a	n/a
39	CTCF	chr5:127169740-127169890	GM12867	blood:	n/a	n/a
40	CTCF	chr5:127180480-127180630	MCF-7	breast:	n/a	n/a
41	CTCF	chr5:127169786-127169850	GM13976	blood:	n/a	n/a
42	CTCF	chr5:127169800-127169950	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr5:127169748-127169947	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr5:127180433-127180542	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:127169783-127169932	GM12878	blood:	n/a	n/a
46	CTCF	chr5:127158273-127158317	Lung_OC	lung:	n/a	n/a
47	CTCF	chr5:127174885-127175024	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr5:127169760-127169910	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr5:127180429-127180593	LNCaP	prostate:	n/a	n/a
50	CTCF	chr5:127169800-127169950	Caco-2	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:127180473-127180523	AG04450	lung:	fetal
2	chr5:127180473-127180523	ovcar-3	ovarian:	n/a
3	chr5:127157258-127157308	NH-A	brain:	n/a
4	chr5:127180473-127180523	HNPCEpiC	eye:	n/a
5	chr5:127180473-127180523	GM12892	blood:	n/a
6	chr5:127157258-127157308	GM12891	blood:	n/a
7	chr5:127157258-127157308	BE2_C	brain:	n/a
8	chr5:127157258-127157308	HEK293	kidney:	embryo
9	chr5:127180473-127180523	GM12891	blood:	n/a
10	chr5:127157258-127157308	SKMC	muscle:	n/a
11	chr5:127157258-127157308	AoSMC	blood vessel:	n/a
12	chr5:127157258-127157308	NT2-D1	testis:	n/a
13	chr5:127157258-127157308	CMK	blood:	n/a
14	chr5:127180473-127180523	IMR90	lung:	fetal
15	chr5:127180473-127180523	HPAEpiC	pulmonary alveolar:	n/a
16	chr5:127157258-127157308	ProgFib	skin:	n/a
17	chr5:127157258-127157308	Hepatocyte	liver:	n/a
18	chr5:127157258-127157308	AG10803	skin:	n/a
19	chr5:127157258-127157308	ovcar-3	ovarian:	n/a
20	chr5:127157258-127157308	HUVEC	blood vessel:	n/a
21	chr5:127180473-127180523	Caco-2	colon:	n/a
22	chr5:127157258-127157308	AG04450	lung:	fetal
23	chr5:127180473-127180523	BJ	skin:	n/a
24	chr5:127157258-127157308	HL-60	blood:	n/a
25	chr5:127180473-127180523	HRE	kidney:	n/a
26	chr5:127157258-127157308	AG09309	skin:	n/a
27	chr5:127180473-127180523	PANC-1	pancreas:	n/a
28	chr5:127180473-127180523	GM19239	blood:	n/a
29	chr5:127180473-127180523	GM06990	blood:	n/a
30	chr5:127180473-127180523	AG10803	skin:	n/a
31	chr5:127180473-127180523	NT2-D1	testis:	n/a
32	chr5:127180473-127180523	Jurkat	blood:	n/a
33	chr5:127157258-127157308	GM19239	blood:	n/a
34	chr5:127157258-127157308	ECC-1	luminal epithelium:	n/a
35	chr5:127157258-127157308	HRCEpiC	kidney:	n/a
36	chr5:127180473-127180523	BE2_C	brain:	n/a
37	chr5:127157258-127157308	SK-N-SH_RA	brain:	n/a
38	chr5:127180473-127180523	U87	brain:	n/a
39	chr5:127180473-127180523	ProgFib	skin:	n/a
40	chr5:127180473-127180523	MCF10A-Er-Src	breast:	n/a
41	chr5:127157258-127157308	MCF-7	breast:	n/a
42	chr5:127157258-127157308	GM06990	blood:	n/a
43	chr5:127157258-127157308	HEEpiC	esophagus:	n/a
44	chr5:127157258-127157308	Jurkat	blood:	n/a
45	chr5:127180473-127180523	SKMC	muscle:	n/a
46	chr5:127180473-127180523	SK-N-SH	brain:	n/a
47	chr5:127157258-127157308	HCPEpiC	choroid plexus:	n/a
48	chr5:127180473-127180523	NHDF-neo	bronchial:	n/a
49	chr5:127157258-127157308	HAEpiC	amniotic membrane:	n/a
50	chr5:127157258-127157308	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:127185753..127187398-chr5:127187424..127189793,2	MCF-7	breast:
2	chr5:127150471..127153155-chr5:127164989..127167539,2	K562	blood:
3	chr5:127186304..127188032-chr5:127417848..127420285,2	MCF-7	breast:
4	chr5:127185753..127187398-chr5:127187424..127189793,2	MCF-7	breast:
5	chr5:127172554..127175217-chr5:127418904..127421266,2	K562	blood:
6	chr5:127186051..127188468-chr5:127192299..127194674,2	MCF-7	breast:
7	chr5:127160237..127162603-chr5:127205633..127207366,2	MCF-7	breast:
8	chr5:127093555..127095381-chr5:127175132..127176761,2	MCF-7	breast:
9	chr5:126899533..126900245-chr5:127196051..127196561,2	K562	blood:
10	chr5:127170472..127172876-chr5:127173742..127176446,2	K562	blood:
11	chr5:127170472..127172876-chr5:127173742..127176446,2	K562	blood:
12	chr5:127193954..127196156-chr5:127196517..127199360,2	MCF-7	breast:
13	chr5:127163372..127165051-chr5:127202469..127205145,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBN2-3	chr5:127193306-127193496	XLOC_004992
2	lnc-FBN2-3	chr5:127174178-127174374	XLOC_004992

Variant related genes	Relation type
ENSG00000250603	TF binding region
ENSG00000250603	CpG island
ENSG00000245937	chromatin interactions
ENSG00000250603	chromatin interactions
ENSG00000064651	chromatin interactions

Extended variants
information (count: 1434 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1434 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs698171	chr5:127156760-127156761	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs80189691	chr5:127156830-127156831	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs569275614	chr5:127156838-127156839	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs529330596	chr5:127156842-127156843	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs532890405	chr5:127156866-127156867	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs542729633	chr5:127156894-127156895	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs559295482	chr5:127156992-127156993	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs528448001	chr5:127157009-127157010	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs79841161	chr5:127157015-127157016	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs571838289	chr5:127157086-127157087	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs531238260	chr5:127157129-127157130	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs199982072	chr5:127157137-127157138	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs567862961	chr5:127157172-127157173	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs73783985	chr5:127157177-127157178	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs555477986	chr5:127157188-127157189	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs528930965	chr5:127157190-127157191	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs370952023	chr5:127157217-127157218	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs185254321	chr5:127157258-127157259	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs189665521	chr5:127157259-127157260	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs577817102	chr5:127157278-127157279	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs543713503	chr5:127157281-127157282	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs556845452	chr5:127157315-127157316	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs573804679	chr5:127157316-127157317	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs542442758	chr5:127157371-127157372	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs375501012	chr5:127157397-127157398	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs140865794	chr5:127157418-127157419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs59790213	chr5:127157427-127157428	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs570667476	chr5:127157470-127157471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs544998573	chr5:127157490-127157491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539349646	chr5:127157724-127157725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537739452	chr5:127157755-127157756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114714199	chr5:127157782-127157783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs150149699	chr5:127157814-127157815	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs145554424	chr5:127157831-127157832	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs567891208	chr5:127157858-127157859	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs557280354	chr5:127157870-127157871	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs530298958	chr5:127157881-127157882	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs547254673	chr5:127157919-127157920	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs181302822	chr5:127157957-127157958	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs140314647	chr5:127157969-127157970	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs557431227	chr5:127158001-127158002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs571238384	chr5:127158047-127158048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs536920991	chr5:127158053-127158054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs557200936	chr5:127158058-127158059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573888148	chr5:127158076-127158077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570977199	chr5:127158077-127158078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536028920	chr5:127158156-127158157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552795803	chr5:127158183-127158184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs368766252	chr5:127158238-127158239	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs545113855	chr5:127158260-127158261	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	16397240	CNVD
Parathyroid adenoma	22454399	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:408 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:127150000-127159400	Weak transcription	Right Atrium	heart
2	chr5:127151000-127159000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:127151000-127161200	Weak transcription	HSMM	muscle
4	chr5:127151200-127156800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr5:127152400-127156800	Weak transcription	Colon Smooth Muscle	Colon
6	chr5:127154600-127158600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr5:127155400-127157200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr5:127156200-127159000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr5:127156400-127157200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr5:127156600-127156800	Enhancers	Fetal Kidney	kidney
11	chr5:127156600-127156800	Enhancers	Rectal Smooth Muscle	rectum
12	chr5:127156600-127156800	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr5:127156600-127156800	Active TSS	A549	lung
14	chr5:127156600-127157000	Enhancers	NHDF-Ad	bronchial
15	chr5:127156600-127157200	Enhancers	Muscle Satellite Cultured Cells	--
16	chr5:127156600-127157400	Enhancers	Fetal Intestine Large	intestine
17	chr5:127156600-127157800	Enhancers	Stomach Mucosa	stomach
18	chr5:127156600-127158600	Enhancers	Primary hematopoietic stem cells	blood
19	chr5:127156800-127157000	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr5:127156800-127157400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr5:127156800-127157400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr5:127156800-127157400	Flanking Active TSS	A549	lung
23	chr5:127156800-127157600	Enhancers	Colon Smooth Muscle	Colon
24	chr5:127156800-127157800	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr5:127156800-127158600	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr5:127156800-127159600	Weak transcription	Rectal Smooth Muscle	rectum
27	chr5:127157000-127157600	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr5:127157000-127161000	Weak transcription	NHDF-Ad	bronchial
29	chr5:127157200-127157400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr5:127157200-127159400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr5:127157200-127159400	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr5:127157400-127157800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr5:127157400-127158000	Enhancers	A549	lung
34	chr5:127157400-127158200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr5:127157600-127166000	Weak transcription	Colon Smooth Muscle	Colon
36	chr5:127157800-127158000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr5:127157800-127158600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr5:127158000-127158200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr5:127158000-127169800	Weak transcription	A549	lung
40	chr5:127158200-127158400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr5:127158200-127158400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr5:127158400-127159000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr5:127158400-127161000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr5:127158600-127158800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
45	chr5:127158600-127160600	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr5:127158800-127159600	Enhancers	Stomach Smooth Muscle	stomach
47	chr5:127159000-127160000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr5:127159000-127160400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr5:127159000-127161800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr5:127159200-127159800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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