Variant report

Variant	esv2761130
Chromosome Location	chr7:6122685-6136863
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:61)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6132523-6132819	HepG2	liver:	n/a	n/a
2	CEBPB	chr7:6134397-6134550	IMR90	lung:	n/a	chr7:6134474-6134485
3	CEBPB	chr7:6136175-6136408	K562	blood:	n/a	chr7:6136278-6136289
4	CEBPB	chr7:6134269-6134562	K562	blood:	n/a	chr7:6134474-6134485
5	CEBPB	chr7:6134326-6134634	K562	blood:	n/a	chr7:6134474-6134485
6	CEBPB	chr7:6134330-6134597	H1-hESC	embryonic stem cell:	n/a	chr7:6134474-6134485
7	CEBPB	chr7:6134417-6134609	A549	lung:	n/a	chr7:6134474-6134485
8	CEBPB	chr7:6134395-6134626	HepG2	liver:	n/a	chr7:6134474-6134485
9	CEBPB	chr7:6136224-6136319	HepG2	liver:	n/a	chr7:6136278-6136289
10	CEBPB	chr7:6134421-6134596	Hela-S3	cervix:	n/a	chr7:6134474-6134485
11	CTCF	chr7:6134320-6134470	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr7:6134280-6134430	GM12871	blood:	n/a	n/a
13	CTCF	chr7:6126247-6126275	GM20000	blood:	n/a	n/a
14	CTCF	chr7:6131672-6131737	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr7:6134340-6134490	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr7:6134280-6134430	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr7:6134315-6134466	K562	blood:	n/a	n/a
18	CTCF	chr7:6134291-6134445	HepG2	liver:	n/a	n/a
19	CTCF	chr7:6134300-6134450	NB4	blood:	n/a	n/a
20	CTCF	chr7:6134329-6134514	K562	blood:	n/a	n/a
21	CTCF	chr7:6134300-6134450	Caco-2	colon:	n/a	n/a
22	CTCF	chr7:6134240-6134390	GM12873	blood:	n/a	n/a
23	CTCF	chr7:6134300-6134450	K562	blood:	n/a	n/a
24	CTCF	chr7:6134260-6134410	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr7:6134280-6134430	GM06990	blood:	n/a	n/a
26	CUX1	chr7:6132501-6132661	K562	blood:	n/a	n/a
27	CUX1	chr7:6131167-6131220	K562	blood:	n/a	n/a
28	EP300	chr7:6127394-6127442	K562	blood:	n/a	n/a
29	FAM48A	chr7:6131190-6131390	GM12878	blood:	n/a	n/a
30	FOS	chr7:6135990-6136108	MCF10A-Er-Src	breast:	n/a	n/a
31	FOXA1	chr7:6132501-6132876	HepG2	liver:	n/a	n/a
32	FOXA1	chr7:6132454-6132826	HepG2	liver:	n/a	n/a
33	FOXA1	chr7:6132472-6132827	HepG2	liver:	n/a	n/a
34	FOXA1	chr7:6132473-6132921	HepG2	liver:	n/a	n/a
35	FOXA2	chr7:6132550-6132798	HepG2	liver:	n/a	n/a
36	HDAC2	chr7:6132563-6132808	HepG2	liver:	n/a	n/a
37	JUND	chr7:6134399-6134508	K562	blood:	n/a	n/a
38	MAFF	chr7:6130432-6130732	HepG2	liver:	n/a	n/a
39	MAFK	chr7:6130411-6130725	HepG2	liver:	n/a	chr7:6130553-6130568 chr7:6130558-6130569 chr7:6130557-6130568 chr7:6130558-6130569 chr7:6130553-6130569 chr7:6130557-6130568 chr7:6130556-6130570
40	MAFK	chr7:6130530-6130575	K562	blood:	n/a	chr7:6130553-6130568 chr7:6130558-6130569 chr7:6130557-6130568 chr7:6130558-6130569 chr7:6130553-6130569 chr7:6130557-6130568 chr7:6130556-6130570
41	MAFK	chr7:6130539-6130683	Hela-S3	cervix:	n/a	chr7:6130553-6130568 chr7:6130558-6130569 chr7:6130557-6130568 chr7:6130558-6130569 chr7:6130553-6130569 chr7:6130557-6130568 chr7:6130556-6130570
42	MAFK	chr7:6130464-6130731	HepG2	liver:	n/a	chr7:6130553-6130568 chr7:6130558-6130569 chr7:6130557-6130568 chr7:6130558-6130569 chr7:6130553-6130569 chr7:6130557-6130568 chr7:6130556-6130570
43	MAFK	chr7:6130457-6130682	IMR90	lung:	n/a	chr7:6130553-6130568 chr7:6130558-6130569 chr7:6130557-6130568 chr7:6130558-6130569 chr7:6130553-6130569 chr7:6130557-6130568 chr7:6130556-6130570
44	MAFK	chr7:6136050-6136190	HepG2	liver:	n/a	n/a
45	MAX	chr7:6132734-6132786	HepG2	liver:	n/a	n/a
46	MAZ	chr7:6136228-6136236	HepG2	liver:	n/a	n/a
47	MYBL2	chr7:6132387-6132925	HepG2	liver:	n/a	n/a
48	MYC	chr7:6136018-6136123	H1-hESC	embryonic stem cell:	n/a	n/a
49	MYC	chr7:6133358-6133548	MCF10A-Er-Src	breast:	n/a	n/a
50	MYC	chr7:6128889-6129060	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6124631-6124681	PANC-1	pancreas:	n/a
2	chr7:6124631-6124681	T-47D	breast:	n/a
3	chr7:6124631-6124681	AG09319	gingival:	n/a
4	chr7:6124631-6124681	ProgFib	skin:	n/a
5	chr7:6124631-6124681	Hela-S3	cervix:	n/a
6	chr7:6124631-6124681	HRPEpiC	eye:	n/a
7	chr7:6124631-6124681	AG04449	skin:	fetal
8	chr7:6124631-6124681	AG10803	skin:	n/a
9	chr7:6124631-6124681	HCPEpiC	choroid plexus:	n/a
10	chr7:6124631-6124681	SK-N-MC	brain:	n/a
11	chr7:6124631-6124681	AoSMC	blood vessel:	n/a
12	chr7:6124631-6124681	SKMC	muscle:	n/a
13	chr7:6124631-6124681	MCF10A-Er-Src	breast:	n/a
14	chr7:6124631-6124681	AG09309	skin:	n/a
15	chr7:6124631-6124681	BE2_C	brain:	n/a
16	chr7:6124631-6124681	IMR90	lung:	fetal
17	chr7:6124631-6124681	NB4	blood:	n/a
18	chr7:6124631-6124681	ovcar-3	ovarian:	n/a
19	chr7:6124631-6124681	HCM	heart:	n/a
20	chr7:6124631-6124681	SK-N-SH	brain:	n/a
21	chr7:6124631-6124681	H1-hESC	embryonic stem cell:	embryo
22	chr7:6124631-6124681	Hepatocyte	liver:	n/a
23	chr7:6124631-6124681	NH-A	brain:	n/a
24	chr7:6124631-6124681	AG04450	lung:	fetal
25	chr7:6124631-6124681	U87	brain:	n/a
26	chr7:6124631-6124681	HMEC	breast:	n/a
27	chr7:6124631-6124681	GM12878	blood:	n/a
28	chr7:6124631-6124681	GM12892	blood:	n/a
29	chr7:6124631-6124681	HPAEpiC	pulmonary alveolar:	n/a
30	chr7:6124631-6124681	MCF-7	breast:	n/a
31	chr7:6124631-6124681	SK-N-SH_RA	brain:	n/a
32	chr7:6124631-6124681	CMK	blood:	n/a
33	chr7:6124631-6124681	GM12891	blood:	n/a
34	chr7:6124631-6124681	HEK293	kidney:	embryo
35	chr7:6124631-6124681	NHBE	bronchial:	n/a
36	chr7:6124631-6124681	K562	blood:	n/a
37	chr7:6124631-6124681	HIPEpiC	eye:	n/a
38	chr7:6124631-6124681	HRCEpiC	kidney:	n/a
39	chr7:6124631-6124681	HAEpiC	amniotic membrane:	n/a
40	chr7:6124631-6124681	HCF	heart:	n/a
41	chr7:6124631-6124681	HepG2	liver:	n/a
42	chr7:6124631-6124681	HNPCEpiC	eye:	n/a
43	chr7:6124631-6124681	GM19239	blood:	n/a
44	chr7:6124631-6124681	RPTEC	kidney:	n/a
45	chr7:6124631-6124681	ECC-1	luminal epithelium:	n/a
46	chr7:6124631-6124681	HEEpiC	esophagus:	n/a
47	chr7:6124631-6124681	GM06990	blood:	n/a
48	chr7:6124631-6124681	SAEC	small airway:	n/a
49	chr7:6124631-6124681	LNCaP	prostate:	n/a
50	chr7:6124631-6124681	Jurkat	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6136281..6138801-chr7:6142810..6145571,2	MCF-7	breast:
2	chr7:6129689..6132230-chr7:6141187..6143186,2	K562	blood:
3	chr7:6134295..6136999-chr7:6143069..6146027,4	MCF-7	breast:
4	chr7:6119410..6124898-chr7:6141396..6145150,7	MCF-7	breast:
5	chr7:6090422..6101465-chr7:6116449..6124326,16	K562	blood:
6	chr7:6132461..6134616-chr7:6143450..6145084,2	K562	blood:
7	chr7:6118943..6121901-chr7:6135468..6137928,2	MCF-7	breast:
8	chr7:6118471..6120891-chr7:6135399..6137782,2	K562	blood:
9	chr7:6118878..6122850-chr7:6140823..6146720,14	MCF-7	breast:
10	chr7:6097164..6099061-chr7:6134553..6137084,2	MCF-7	breast:
11	chr7:6134399..6135940-chr7:6137950..6139940,2	K562	blood:
12	chr7:6120819..6122928-chr7:6131075..6133699,2	K562	blood:
13	chr7:6097434..6099559-chr7:6134440..6137386,2	K562	blood:
14	chr7:6130749..6132668-chr7:6140261..6142428,2	MCF-7	breast:
15	chr7:6133404..6135856-chr7:6136642..6138588,2	MCF-7	breast:
16	chr7:6095667..6100309-chr7:6118978..6123029,12	MCF-7	breast:
17	chr7:6127500..6130529-chr7:6140681..6143799,3	MCF-7	breast:
18	chr7:6133404..6135856-chr7:6136642..6138588,2	MCF-7	breast:
19	chr7:6118962..6122557-chr7:6124155..6128114,4	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP42-5	chr7:6124455-6124733	NONHSAT118978
2	lnc-USP42-4	chr7:6128922-6129206	NONHSAT118979
3	lnc-USP42-2	chr7:6131319-6131626	NONHSAT118981
4	lnc-USP42-1	chr7:6124060-6124303	XLOC_005979
5	lnc-USP42-1	chr7:6128421-6128531	XLOC_005979
6	lnc-USP42-1	chr7:6123963-6124367	NONHSAT118977
7	lnc-USP42-1	chr7:6128421-6128531	XLOC_005979
8	lnc-USP42-1	chr7:6124060-6124243	XLOC_005979
9	lnc-USP42-3	chr7:6130515-6131250	NONHSAT118980
10	lnc-USP42-1	chr7:6124776-6124887	XLOC_005979
11	lnc-USP42-1	chr7:6132660-6132716	XLOC_005979
12	lnc-USP42-1	chr7:6124060-6124303	XLOC_005979
13	lnc-USP42-1	chr7:6132660-6132683	XLOC_005979
14	lnc-USP42-1	chr7:6124060-6124303	XLOC_005979

No data

Variant related genes	Relation type
ENSG00000264605	TF binding region
ENSG00000264605	CpG island
ENSG00000086232	chromatin interactions
ENSG00000231704	chromatin interactions
ENSG00000106346	chromatin interactions
ENSG00000252929	chromatin interactions
ENSG00000264605	chromatin interactions
LIN28B	miRNA target sites
IPPK	miRNA target sites
BCL2L11	miRNA target sites
NIN	miRNA target sites

Extended variants
information (count: 527 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:527 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372540487	chr7:6122702-6122703	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs10282134	chr7:6122719-6122720	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs529459924	chr7:6122758-6122759	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs541285831	chr7:6122822-6122823	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs200609357	chr7:6122855-6122856	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs537755339	chr7:6122893-6122894	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs371456221	chr7:6122894-6122895	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs537586814	chr7:6122901-6122902	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs559621667	chr7:6122915-6122916	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs184263813	chr7:6122952-6122953	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs527910849	chr7:6122972-6122973	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs551519148	chr7:6123001-6123002	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs188684040	chr7:6123006-6123007	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs150406216	chr7:6123007-6123008	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs181249104	chr7:6123122-6123123	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs377063477	chr7:6123139-6123140	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs530882351	chr7:6123208-6123209	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs549472763	chr7:6123249-6123250	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs568222646	chr7:6123308-6123309	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs377309106	chr7:6123309-6123310	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs535651187	chr7:6123310-6123311	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs554107407	chr7:6123383-6123384	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs370929112	chr7:6123395-6123396	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs539400448	chr7:6123400-6123401	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs138202685	chr7:6123403-6123404	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs576008744	chr7:6123410-6123411	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs34199446	chr7:6123432-6123433	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs543114872	chr7:6123434-6123435	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs118035543	chr7:6123443-6123444	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs573848924	chr7:6123520-6123521	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs541273823	chr7:6123550-6123551	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs149171993	chr7:6123559-6123560	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs564671815	chr7:6123594-6123595	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs533485471	chr7:6123619-6123620	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs186281214	chr7:6123683-6123684	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs531683072	chr7:6123709-6123710	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs563501674	chr7:6123713-6123714	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs189194151	chr7:6123714-6123715	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs549913764	chr7:6123795-6123796	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs180721073	chr7:6123815-6123816	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs567809075	chr7:6123849-6123850	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs374573042	chr7:6123852-6123853	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs529093930	chr7:6123882-6123883	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs547644141	chr7:6123893-6123894	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs568504690	chr7:6123894-6123895	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs539324140	chr7:6123902-6123903	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs113343987	chr7:6123966-6123967	Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs575570328	chr7:6123988-6123989	Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs569509244	chr7:6124034-6124035	Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
50	rs112871157	chr7:6124035-6124036	Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6121600-6123400	Weak transcription	Placenta	Placenta
2	chr7:6123400-6125000	Enhancers	Placenta	Placenta
3	chr7:6131400-6131600	Enhancers	K562	blood
4	chr7:6131600-6132600	Weak transcription	K562	blood
5	chr7:6132000-6133200	Enhancers	HepG2	liver
6	chr7:6132200-6132400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
7	chr7:6132400-6132600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr7:6132400-6132600	Enhancers	A549	lung
9	chr7:6132400-6132800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr7:6132400-6133000	Enhancers	Hela-S3	cervix
11	chr7:6132600-6132800	Flanking Active TSS	A549	lung
12	chr7:6132600-6132800	Enhancers	K562	blood
13	chr7:6132600-6133200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr7:6132600-6133200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr7:6133000-6142400	Weak transcription	Hela-S3	cervix

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