Variant report

Variant	nsv607714
Chromosome Location	chr7:84213008-84296561
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:443)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:443 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	ATF1	chr7:84259630-84259842	K562	blood:	n/a	n/a
3	ATF1	chr7:84292651-84292819	K562	blood:	n/a	n/a
4	BHLHE40	chr7:84244524-84244740	K562	blood:	n/a	n/a
5	CBX3	chr7:84261530-84261866	K562	blood:	n/a	n/a
6	CBX3	chr7:84232979-84233116	K562	blood:	n/a	n/a
7	CCNT2	chr7:84255504-84255628	K562	blood:	n/a	n/a
8	CEBPB	chr7:84291880-84292238	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr7:84230169-84230320	HepG2	liver:	n/a	n/a
10	CEBPB	chr7:84292623-84292932	IMR90	lung:	n/a	chr7:84292775-84292786
11	CEBPB	chr7:84288191-84288351	IMR90	lung:	n/a	chr7:84288241-84288254
12	CEBPB	chr7:84277157-84277928	IMR90	lung:	n/a	n/a
13	CEBPB	chr7:84292712-84292904	HepG2	liver:	n/a	chr7:84292775-84292786
14	CEBPB	chr7:84288118-84288391	K562	blood:	n/a	chr7:84288241-84288254
15	CTCF	chr7:84244198-84244480	K562	blood:	n/a	n/a
16	CTCF	chr7:84266660-84266810	HMEC	breast:	n/a	n/a
17	CTCF	chr7:84244260-84244389	K562	blood:	n/a	n/a
18	CTCF	chr7:84266474-84266649	MCF-7	breast:	n/a	n/a
19	CTCF	chr7:84266440-84266590	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr7:84244220-84244370	SAEC	small airway:	n/a	n/a
21	CTCF	chr7:84244440-84244590	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr7:84244200-84244350	HPF	lung:	n/a	n/a
23	CTCF	chr7:84244240-84244390	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr7:84266475-84266711	Gliobla	brain:	n/a	n/a
25	CTCF	chr7:84266505-84266650	NHEK	skin:	n/a	n/a
26	CTCF	chr7:84244480-84244630	HRE	kidney:	n/a	n/a
27	CTCF	chr7:84244000-84244150	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr7:84244200-84244350	HCM	heart:	n/a	n/a
29	CTCF	chr7:84266440-84266590	HCT-116	colon:	n/a	n/a
30	CTCF	chr7:84266820-84266970	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr7:84261297-84261397	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr7:84244291-84244333	LNCaP	prostate:	n/a	n/a
33	CTCF	chr7:84266540-84266690	GM12869	blood:	n/a	n/a
34	CTCF	chr7:84243980-84244130	WI-38	lung:	n/a	n/a
35	CTCF	chr7:84244070-84244629	HCT-116	colon:	n/a	n/a
36	CTCF	chr7:84244240-84244390	BE2_C	brain:	n/a	n/a
37	CTCF	chr7:84244307-84244357	GM12878	blood:	n/a	n/a
38	CTCF	chr7:84266560-84266710	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr7:84244280-84244430	HFF	foreskin:	n/a	n/a
40	CTCF	chr7:84266460-84266610	GM12872	blood:	n/a	n/a
41	CTCF	chr7:84228835-84228906	LNCaP	prostate:	n/a	n/a
42	CTCF	chr7:84266480-84266630	GM12873	blood:	n/a	n/a
43	CTCF	chr7:84244300-84244450	AG10803	skin:	n/a	n/a
44	CTCF	chr7:84244207-84244440	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr7:84244280-84244430	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr7:84266400-84266550	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr7:84266500-84266619	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:84232860-84233010	K562	blood:	n/a	n/a
49	CTCF	chr7:84251740-84251890	NHEK	skin:	n/a	n/a
50	CTCF	chr7:84266720-84266870	AG04449	skin:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:84267140-84267190	GM12892	blood:	n/a
2	chr7:84267140-84267190	Hela-S3	cervix:	n/a
3	chr7:84267140-84267190	MCF-7	breast:	n/a
4	chr7:84267140-84267190	HL-60	blood:	n/a
5	chr7:84277775-84277825	HPAEpiC	pulmonary alveolar:	n/a
6	chr7:84277775-84277825	HAEpiC	amniotic membrane:	n/a
7	chr7:84277775-84277825	HNPCEpiC	eye:	n/a
8	chr7:84277775-84277825	PrEC	prostate:	n/a
9	chr7:84277775-84277825	Jurkat	blood:	n/a
10	chr7:84267140-84267190	NB4	blood:	n/a
11	chr7:84277775-84277825	ovcar-3	ovarian:	n/a
12	chr7:84267140-84267190	AG09319	gingival:	n/a
13	chr7:84277775-84277825	SAEC	small airway:	n/a
14	chr7:84277775-84277825	Caco-2	colon:	n/a
15	chr7:84267140-84267190	NT2-D1	testis:	n/a
16	chr7:84267140-84267190	GM19239	blood:	n/a
17	chr7:84267140-84267190	BE2_C	brain:	n/a
18	chr7:84277775-84277825	RPTEC	kidney:	n/a
19	chr7:84277775-84277825	BE2_C	brain:	n/a
20	chr7:84277775-84277825	HCF	heart:	n/a
21	chr7:84277775-84277825	GM12892	blood:	n/a
22	chr7:84277775-84277825	U87	brain:	n/a
23	chr7:84267140-84267190	CMK	blood:	n/a
24	chr7:84267140-84267190	AG09309	skin:	n/a
25	chr7:84267140-84267190	H1-hESC	embryonic stem cell:	embryo
26	chr7:84267140-84267190	LNCaP	prostate:	n/a
27	chr7:84267140-84267190	SK-N-SH_RA	brain:	n/a
28	chr7:84267140-84267190	RPTEC	kidney:	n/a
29	chr7:84277775-84277825	GM12891	blood:	n/a
30	chr7:84277775-84277825	NH-A	brain:	n/a
31	chr7:84277775-84277825	HUVEC	blood vessel:	n/a
32	chr7:84267140-84267190	SK-N-SH	brain:	n/a
33	chr7:84267140-84267190	HEK293	kidney:	embryo
34	chr7:84277775-84277825	PFSK-1	brain:	n/a
35	chr7:84267140-84267190	T-47D	breast:	n/a
36	chr7:84277775-84277825	HL-60	blood:	n/a
37	chr7:84267140-84267190	ProgFib	skin:	n/a
38	chr7:84277775-84277825	AG09309	skin:	n/a
39	chr7:84267140-84267190	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:84267140-84267190	HRCEpiC	kidney:	n/a
41	chr7:84277775-84277825	SK-N-SH_RA	brain:	n/a
42	chr7:84277775-84277825	AG04450	lung:	fetal
43	chr7:84267140-84267190	NH-A	brain:	n/a
44	chr7:84277775-84277825	Hepatocyte	liver:	n/a
45	chr7:84277775-84277825	HRE	kidney:	n/a
46	chr7:84277775-84277825	GM19239	blood:	n/a
47	chr7:84267140-84267190	HCF	heart:	n/a
48	chr7:84267140-84267190	A549	lung:	n/a
49	chr7:84277775-84277825	HEEpiC	esophagus:	n/a
50	chr7:84267140-84267190	HRPEpiC	eye:	n/a

(count:17 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRM3-2	chr7:84213467-84213634	NR_110080
2	lnc-GRM3-2	chr7:84213467-84213638	XLOC_006159
3	lnc-GRM3-2	chr7:84213466-84213638	NONHSAT121790

No data

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

Extended variants
information (count: 2120 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2120 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143494134	chr7:84213595-84213596	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs181674599	chr7:84217686-84217687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533921581	chr7:84217691-84217692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149779337	chr7:84217712-84217713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144724105	chr7:84217757-84217758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs386715355	chr7:84217784-84217785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114845809	chr7:84217785-84217786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs574798890	chr7:84217800-84217801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145230983	chr7:84217832-84217833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554164001	chr7:84217972-84217973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572331482	chr7:84217986-84217987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185975404	chr7:84218030-84218031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564429067	chr7:84218071-84218072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190081641	chr7:84218100-84218101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370358112	chr7:84218113-84218114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs12670015	chr7:84218119-84218120	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs181317818	chr7:84218146-84218147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529571457	chr7:84218241-84218242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547759534	chr7:84218269-84218270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560134725	chr7:84218316-84218317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539235721	chr7:84218331-84218332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374405165	chr7:84218362-84218363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527286855	chr7:84218370-84218371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552104632	chr7:84218377-84218378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs34283382	chr7:84218386-84218387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs1989900	chr7:84218397-84218398	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs147615263	chr7:84218402-84218403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550022256	chr7:84218405-84218406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568237185	chr7:84218445-84218446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566081524	chr7:84218456-84218457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140566502	chr7:84218467-84218468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553771003	chr7:84218478-84218479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572447293	chr7:84218488-84218489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539462054	chr7:84218511-84218512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs144530353	chr7:84218513-84218514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs882625	chr7:84218537-84218538	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs543491488	chr7:84218578-84218579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs151134881	chr7:84218659-84218660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140073929	chr7:84218723-84218724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs73712978	chr7:84218726-84218727	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs372503730	chr7:84218775-84218776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533634480	chr7:84218779-84218780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185498822	chr7:84218809-84218810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs80230043	chr7:84218844-84218845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576661859	chr7:84218853-84218854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs117528957	chr7:84218880-84218881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200079600	chr7:84218910-84218911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10226986	chr7:84218930-84218931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190591899	chr7:84218932-84218933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs143384470	chr7:84218944-84218945	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:260 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84217600-84219400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr7:84218000-84219200	Enhancers	NHEK	skin
3	chr7:84218000-84219400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr7:84218200-84219000	Enhancers	HMEC	breast
5	chr7:84218400-84219000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:84232600-84233000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:84241800-84245000	Enhancers	NHDF-Ad	bronchial
8	chr7:84242200-84242600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr7:84242200-84244600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:84242200-84244800	Enhancers	Fetal Lung	lung
11	chr7:84242600-84242800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr7:84242800-84245000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr7:84244200-84245000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr7:84244600-84245000	Enhancers	HUVEC	blood vessel
15	chr7:84245000-84250000	Weak transcription	NHDF-Ad	bronchial
16	chr7:84246600-84247200	Enhancers	Osteobl	bone
17	chr7:84250000-84250800	Enhancers	NHDF-Ad	bronchial
18	chr7:84250800-84252600	Weak transcription	NHDF-Ad	bronchial
19	chr7:84252600-84254800	Enhancers	NHDF-Ad	bronchial
20	chr7:84252800-84253400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr7:84252800-84254400	Enhancers	Osteobl	bone
22	chr7:84253000-84254600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:84254400-84266600	Weak transcription	Osteobl	bone
24	chr7:84254800-84256600	Weak transcription	NHDF-Ad	bronchial
25	chr7:84256400-84257000	Enhancers	NHLF	lung
26	chr7:84256600-84257200	Enhancers	NHDF-Ad	bronchial
27	chr7:84257200-84257800	Weak transcription	NHDF-Ad	bronchial
28	chr7:84257800-84258000	Enhancers	NHDF-Ad	bronchial
29	chr7:84258400-84260800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr7:84261400-84261800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:84261800-84262400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr7:84262200-84266800	Weak transcription	Right Atrium	heart
33	chr7:84262400-84262800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr7:84262800-84266800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr7:84263800-84266800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:84264200-84266400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr7:84264400-84266400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr7:84265200-84265600	Enhancers	HUVEC	blood vessel
39	chr7:84265600-84266000	Weak transcription	HUVEC	blood vessel
40	chr7:84265800-84266200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr7:84266000-84269200	Enhancers	HUVEC	blood vessel
42	chr7:84266200-84266600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr7:84266200-84266800	Enhancers	HSMM	muscle
44	chr7:84266200-84266800	ZNF genes & repeats	NHEK	skin
45	chr7:84266200-84267200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr7:84266200-84268600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr7:84266400-84266800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr7:84266400-84267000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:84266400-84267000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr7:84266400-84267200	Enhancers	Lung	lung

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