Variant report

Variant	nsv525826
Chromosome Location	chr7:84186159-84302877
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:528)
CpG islands
(count:123)
Chromatin interactive
region (count:23)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:528 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:84287580-84287954	K562	blood:	n/a	n/a
2	ARID3A	chr7:84302368-84302402	K562	blood:	n/a	n/a
3	ATF1	chr7:84298510-84298929	K562	blood:	n/a	n/a
4	ATF1	chr7:84292651-84292819	K562	blood:	n/a	n/a
5	ATF1	chr7:84259630-84259842	K562	blood:	n/a	n/a
6	BHLHE40	chr7:84244524-84244740	K562	blood:	n/a	n/a
7	BRCA1	chr7:84302255-84302599	GM12878	blood:	n/a	n/a
8	CBX3	chr7:84232979-84233116	K562	blood:	n/a	n/a
9	CBX3	chr7:84261530-84261866	K562	blood:	n/a	n/a
10	CCNT2	chr7:84255504-84255628	K562	blood:	n/a	n/a
11	CCNT2	chr7:84298566-84298780	K562	blood:	n/a	n/a
12	CEBPB	chr7:84288118-84288391	K562	blood:	n/a	chr7:84288241-84288254
13	CEBPB	chr7:84302634-84302785	HepG2	liver:	n/a	chr7:84302754-84302765
14	CEBPB	chr7:84288191-84288351	IMR90	lung:	n/a	chr7:84288241-84288254
15	CEBPB	chr7:84292712-84292904	HepG2	liver:	n/a	chr7:84292775-84292786
16	CEBPB	chr7:84292623-84292932	IMR90	lung:	n/a	chr7:84292775-84292786
17	CEBPB	chr7:84291880-84292238	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr7:84230169-84230320	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:84277157-84277928	IMR90	lung:	n/a	n/a
20	CTCF	chr7:84266901-84267039	Fibrobl	skin:	n/a	n/a
21	CTCF	chr7:84244240-84244390	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr7:84251740-84251890	NHEK	skin:	n/a	n/a
23	CTCF	chr7:84222146-84222190	LNCaP	prostate:	n/a	n/a
24	CTCF	chr7:84266556-84266598	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr7:84244240-84244390	MCF-7	breast:	n/a	n/a
26	CTCF	chr7:84266475-84266711	Gliobla	brain:	n/a	n/a
27	CTCF	chr7:84266440-84266590	GM12875	blood:	n/a	n/a
28	CTCF	chr7:84266540-84266690	GM12869	blood:	n/a	n/a
29	CTCF	chr7:84266460-84266610	A549	lung:	n/a	n/a
30	CTCF	chr7:84244200-84244350	HCM	heart:	n/a	n/a
31	CTCF	chr7:84244240-84244390	SAEC	small airway:	n/a	n/a
32	CTCF	chr7:84266400-84266550	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr7:84266440-84266590	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr7:84244280-84244430	Caco-2	colon:	n/a	n/a
35	CTCF	chr7:84301477-84301481	Fibrobl	skin:	n/a	n/a
36	CTCF	chr7:84244220-84244370	SAEC	small airway:	n/a	n/a
37	CTCF	chr7:84244220-84244370	HMF	breast:	n/a	n/a
38	CTCF	chr7:84266600-84266750	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr7:84266660-84266810	HMEC	breast:	n/a	n/a
40	CTCF	chr7:84244180-84244330	MCF-7	breast:	n/a	n/a
41	CTCF	chr7:84244085-84244584	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:84237480-84237630	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr7:84244280-84244430	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr7:84244070-84244629	HCT-116	colon:	n/a	n/a
45	CTCF	chr7:84266474-84266649	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:84266460-84266610	BE2_C	brain:	n/a	n/a
47	CTCF	chr7:84296060-84296210	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:84244220-84244370	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr7:84244200-84244350	HPF	lung:	n/a	n/a
50	CTCF	chr7:84244195-84244420	MCF-7	breast:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:84277775-84277825	AG09319	gingival:	n/a
2	chr7:84277775-84277825	AG09319	gingival:	n/a
3	chr7:84277775-84277825	MCF-7	breast:	n/a
4	chr7:84277775-84277825	PrEC	prostate:	n/a
5	chr7:84277775-84277825	PANC-1	pancreas:	n/a
6	chr7:84277775-84277825	GM12891	blood:	n/a
7	chr7:84267140-84267190	PANC-1	pancreas:	n/a
8	chr7:84277775-84277825	ovcar-3	ovarian:	n/a
9	chr7:84267140-84267190	HCM	heart:	n/a
10	chr7:84267140-84267190	HCT-116	colon:	n/a
11	chr7:84267140-84267190	MCF-7	breast:	n/a
12	chr7:84267140-84267190	ECC-1	luminal epithelium:	n/a
13	chr7:84277775-84277825	HCM	heart:	n/a
14	chr7:84277775-84277825	HAEpiC	amniotic membrane:	n/a
15	chr7:84277775-84277825	NT2-D1	testis:	n/a
16	chr7:84277775-84277825	HIPEpiC	eye:	n/a
17	chr7:84277775-84277825	AG04449	skin:	fetal
18	chr7:84277775-84277825	NHBE	bronchial:	n/a
19	chr7:84277775-84277825	RPTEC	kidney:	n/a
20	chr7:84277775-84277825	HCPEpiC	choroid plexus:	n/a
21	chr7:84267140-84267190	ProgFib	skin:	n/a
22	chr7:84267140-84267190	BJ	skin:	n/a
23	chr7:84277775-84277825	HRPEpiC	eye:	n/a
24	chr7:84267140-84267190	AG04449	skin:	fetal
25	chr7:84267140-84267190	CMK	blood:	n/a
26	chr7:84277775-84277825	HCT-116	colon:	n/a
27	chr7:84267140-84267190	U87	brain:	n/a
28	chr7:84277775-84277825	LNCaP	prostate:	n/a
29	chr7:84277775-84277825	GM19239	blood:	n/a
30	chr7:84277775-84277825	GM12878	blood:	n/a
31	chr7:84267140-84267190	HL-60	blood:	n/a
32	chr7:84267140-84267190	LNCaP	prostate:	n/a
33	chr7:84267140-84267190	GM12892	blood:	n/a
34	chr7:84267140-84267190	Hela-S3	cervix:	n/a
35	chr7:84277775-84277825	SK-N-SH_RA	brain:	n/a
36	chr7:84277775-84277825	GM06990	blood:	n/a
37	chr7:84277775-84277825	HUVEC	blood vessel:	n/a
38	chr7:84267140-84267190	PFSK-1	brain:	n/a
39	chr7:84277775-84277825	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:84277775-84277825	NH-A	brain:	n/a
41	chr7:84277775-84277825	SAEC	small airway:	n/a
42	chr7:84267140-84267190	H1-hESC	embryonic stem cell:	embryo
43	chr7:84267140-84267190	K562	blood:	n/a
44	chr7:84277775-84277825	CMK	blood:	n/a
45	chr7:84267140-84267190	NB4	blood:	n/a
46	chr7:84277775-84277825	HMEC	breast:	n/a
47	chr7:84267140-84267190	AG04450	lung:	fetal
48	chr7:84277775-84277825	HRE	kidney:	n/a
49	chr7:84277775-84277825	HEK293	kidney:	embryo
50	chr7:84277775-84277825	Caco-2	colon:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:84231197..84234055-chr7:84234117..84236974,2	K562	blood:
2	chr3:161089345..161090957-chr7:84248345..84250491,2	MCF-7	breast:
3	chr7:84215550..84219199-chr7:84222001..84225003,3	K562	blood:
4	chr7:84273543..84275443-chr7:84283712..84286350,2	K562	blood:
5	chr7:84297350..84299613-chr7:84307072..84309162,2	K562	blood:
6	chr7:84297350..84299961-chr7:84307072..84309162,3	K562	blood:
7	chr7:84250435..84252517-chr7:84252923..84255018,2	K562	blood:
8	chr7:84293189..84295299-chr7:84297078..84299323,2	K562	blood:
9	chr7:84302626..84304689-chr7:84308409..84311060,2	MCF-7	breast:
10	chr7:84275439..84277976-chr7:84279778..84282553,2	K562	blood:
11	chr7:84158595..84159433-chr7:84240484..84241224,2	MCF-7	breast:
12	chr7:84158367..84158951-chr7:84240610..84241382,2	MCF-7	breast:
13	chr17:56736359..56736893-chr7:84265214..84266196,2	MCF-7	breast:
14	chr7:84293189..84295299-chr7:84297078..84299323,2	K562	blood:
15	chr7:84250435..84252517-chr7:84252923..84255018,2	K562	blood:
16	chr7:84243619..84244378-chr7:84650207..84650987,2	MCF-7	breast:
17	chr7:84273543..84275443-chr7:84283712..84286350,2	K562	blood:
18	chr7:84244149..84244717-chr7:84651890..84652789,2	MCF-7	breast:
19	chr7:84231197..84234055-chr7:84234117..84236974,2	K562	blood:
20	chr7:84215550..84219199-chr7:84222001..84225003,3	K562	blood:
21	chr7:84298376..84301290-chr7:84302394..84304217,2	MCF-7	breast:
22	chr7:84275439..84277976-chr7:84279778..84282553,2	K562	blood:
23	chr7:84298376..84301290-chr7:84302394..84304217,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRM3-2	chr7:84200295-84200423	NR_110080
2	lnc-GRM3-2	chr7:84200295-84204159	XLOC_006159
3	lnc-GRM3-2	chr7:84200294-84200423	NONHSAT121790
4	lnc-GRM3-2	chr7:84213466-84213638	NONHSAT121790
5	lnc-GRM3-2	chr7:84200295-84200423	XLOC_006159
6	lnc-GRM3-2	chr7:84213467-84213638	XLOC_006159
7	lnc-GRM3-2	chr7:84213467-84213634	NR_110080

No data

Variant related genes	Relation type
ENSG00000265050	TF binding region
ENSG00000265050	CpG island
ENSG00000196542	chromatin interactions
ENSG00000202077	chromatin interactions
ARHGAP1	miRNA target sites
ARFIP1	miRNA target sites

Extended variants
information (count: 2738 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2738 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2214308	chr7:84186159-84186160	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557127454	chr7:84186209-84186210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568663142	chr7:84186220-84186221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570300282	chr7:84186243-84186244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2188985	chr7:84186245-84186246	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs572932803	chr7:84186263-84186264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369419774	chr7:84186282-84186283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186461515	chr7:84186322-84186323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149070757	chr7:84186325-84186326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116232059	chr7:84186455-84186456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544341042	chr7:84186467-84186468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563101827	chr7:84186530-84186531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566252345	chr7:84186547-84186548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553124587	chr7:84186548-84186549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530288832	chr7:84186581-84186582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369576118	chr7:84186617-84186618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190452704	chr7:84186637-84186638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs560745677	chr7:84186735-84186736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183750853	chr7:84186785-84186786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528139678	chr7:84186789-84186790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78428129	chr7:84186792-84186793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187839120	chr7:84186795-84186796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527461459	chr7:84188428-84188429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377231327	chr7:84188437-84188438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs552479310	chr7:84188480-84188481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192850195	chr7:84188483-84188484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538278447	chr7:84188522-84188523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs370530112	chr7:84188573-84188574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138207468	chr7:84188594-84188595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568415561	chr7:84188606-84188607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs532881041	chr7:84188613-84188614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552924004	chr7:84188647-84188648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535974533	chr7:84188662-84188663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs116328178	chr7:84188688-84188689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572633235	chr7:84188703-84188704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185347439	chr7:84188722-84188723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189510448	chr7:84188742-84188743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576657288	chr7:84188794-84188795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575278120	chr7:84190610-84190611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77622148	chr7:84190631-84190632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs150522925	chr7:84190649-84190650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192351393	chr7:84190684-84190685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183351095	chr7:84190714-84190715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139489439	chr7:84190744-84190745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs187073270	chr7:84190778-84190779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563419906	chr7:84190879-84190880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531057843	chr7:84190903-84190904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs549156962	chr7:84190935-84190936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567473471	chr7:84190953-84190954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs544271502	chr7:84190955-84190956	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84182000-84186800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:84188400-84188800	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr7:84190600-84191400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:84191000-84191600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:84191200-84191600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr7:84191400-84194400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr7:84194200-84194800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr7:84194400-84194800	Enhancers	H9 Cell Line	embryonic stem cell
9	chr7:84194400-84194800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr7:84194400-84195000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr7:84194400-84195200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:84194400-84195200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:84194400-84195200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:84195200-84196400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr7:84196600-84196800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:84197800-84198000	Enhancers	NHDF-Ad	bronchial
17	chr7:84198000-84198400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr7:84198000-84198400	Active TSS	Breast Myoepithelial Primary Cells	Breast
19	chr7:84198000-84198600	Active TSS	NHDF-Ad	bronchial
20	chr7:84198400-84198600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr7:84212200-84212800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr7:84217600-84219400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr7:84218000-84219200	Enhancers	NHEK	skin
24	chr7:84218000-84219400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr7:84218200-84219000	Enhancers	HMEC	breast
26	chr7:84218400-84219000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr7:84232600-84233000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr7:84241800-84245000	Enhancers	NHDF-Ad	bronchial
29	chr7:84242200-84242600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:84242200-84244600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr7:84242200-84244800	Enhancers	Fetal Lung	lung
32	chr7:84242600-84242800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr7:84242800-84245000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr7:84244200-84245000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr7:84244600-84245000	Enhancers	HUVEC	blood vessel
36	chr7:84245000-84250000	Weak transcription	NHDF-Ad	bronchial
37	chr7:84246600-84247200	Enhancers	Osteobl	bone
38	chr7:84250000-84250800	Enhancers	NHDF-Ad	bronchial
39	chr7:84250800-84252600	Weak transcription	NHDF-Ad	bronchial
40	chr7:84252600-84254800	Enhancers	NHDF-Ad	bronchial
41	chr7:84252800-84253400	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr7:84252800-84254400	Enhancers	Osteobl	bone
43	chr7:84253000-84254600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr7:84254400-84266600	Weak transcription	Osteobl	bone
45	chr7:84254800-84256600	Weak transcription	NHDF-Ad	bronchial
46	chr7:84256400-84257000	Enhancers	NHLF	lung
47	chr7:84256600-84257200	Enhancers	NHDF-Ad	bronchial
48	chr7:84257200-84257800	Weak transcription	NHDF-Ad	bronchial
49	chr7:84257800-84258000	Enhancers	NHDF-Ad	bronchial
50	chr7:84258400-84260800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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