Variant report

Variant	nsv1021479
Chromosome Location	chr7:19363947-19485519
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:492)
CpG islands
(count:244)
Chromatin interactive
region (count:5)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:492 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr7:19444572-19445053	A549	lung:	n/a	n/a
2	ATF3	chr7:19444493-19444867	A549	lung:	n/a	n/a
3	ATF3	chr7:19401699-19402094	HCT-116	colon:	n/a	n/a
4	BCL3	chr7:19444394-19444990	A549	lung:	n/a	chr7:19444641-19444650
5	BHLHE40	chr7:19437440-19437816	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:19422585-19422633	GM12878	blood:	n/a	n/a
7	CBX3	chr7:19444505-19444941	HCT-116	colon:	n/a	n/a
8	CEBPB	chr7:19444404-19445628	A549	lung:	n/a	chr7:19445336-19445347
9	CEBPB	chr7:19446082-19446303	A549	lung:	n/a	n/a
10	CEBPB	chr7:19444478-19444920	A549	lung:	n/a	n/a
11	CEBPB	chr7:19379927-19380128	A549	lung:	n/a	n/a
12	CEBPB	chr7:19368409-19368599	HepG2	liver:	n/a	chr7:19368529-19368542 chr7:19368530-19368541 chr7:19368529-19368540
13	CEBPB	chr7:19379888-19380200	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr7:19444511-19445576	Hela-S3	cervix:	n/a	chr7:19445336-19445347
15	CEBPB	chr7:19406922-19407130	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr7:19445213-19445455	HepG2	liver:	n/a	chr7:19445336-19445347
17	CEBPB	chr7:19431952-19432321	IMR90	lung:	n/a	n/a
18	CEBPB	chr7:19401785-19402098	IMR90	lung:	n/a	n/a
19	CEBPB	chr7:19444429-19445027	HCT-116	colon:	n/a	n/a
20	CEBPB	chr7:19477072-19477270	IMR90	lung:	n/a	n/a
21	CEBPB	chr7:19445196-19445500	A549	lung:	n/a	chr7:19445336-19445347
22	CEBPB	chr7:19445197-19445390	K562	blood:	n/a	chr7:19445336-19445347
23	CEBPB	chr7:19379880-19380108	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:19401780-19402111	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr7:19372759-19372985	IMR90	lung:	n/a	chr7:19372865-19372873 chr7:19372900-19372913
26	CEBPB	chr7:19444492-19445539	IMR90	lung:	n/a	chr7:19445336-19445347
27	CHD2	chr7:19444604-19444999	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr7:19483786-19483981	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr7:19481884-19482109	A549	lung:	n/a	n/a
30	CTCF	chr7:19481999-19482011	K562	blood:	n/a	n/a
31	CTCF	chr7:19481920-19482070	GM12871	blood:	n/a	n/a
32	CTCF	chr7:19414707-19414785	ProgFib	skin:	n/a	n/a
33	CTCF	chr7:19481900-19482050	MCF-7	breast:	n/a	n/a
34	CTCF	chr7:19481839-19482147	T-47D	breast:	n/a	n/a
35	CTCF	chr7:19481900-19482050	HCM	heart:	n/a	n/a
36	CTCF	chr7:19481960-19482110	HAc	cerebellar:	n/a	n/a
37	CTCF	chr7:19481880-19482030	AG04450	lung:	n/a	n/a
38	CTCF	chr7:19481920-19482059	HepG2	liver:	n/a	n/a
39	CTCF	chr7:19481894-19482097	NHEK	skin:	n/a	n/a
40	CTCF	chr7:19481874-19482092	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr7:19481884-19482148	ProgFib	skin:	n/a	n/a
42	CTCF	chr7:19481940-19482090	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr7:19481960-19482110	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr7:19482160-19482310	GM12865	blood:	n/a	n/a
45	CTCF	chr7:19481940-19482090	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr7:19481940-19482090	HRE	kidney:	n/a	n/a
47	CTCF	chr7:19481959-19482062	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:19481940-19482090	AG09309	skin:	n/a	n/a
49	CTCF	chr7:19481900-19482050	HMEC	breast:	n/a	n/a
50	CTCF	chr7:19481926-19482077	GM13977	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:19453933-19453983	HAEpiC	amniotic membrane:	n/a
2	chr7:19417585-19417635	RPTEC	kidney:	n/a
3	chr7:19443825-19443875	HRE	kidney:	n/a
4	chr7:19443825-19443875	LNCaP	prostate:	n/a
5	chr7:19408343-19408393	T-47D	breast:	n/a
6	chr7:19408343-19408393	PrEC	prostate:	n/a
7	chr7:19417585-19417635	HRCEpiC	kidney:	n/a
8	chr7:19443825-19443875	SK-N-MC	brain:	n/a
9	chr7:19417585-19417635	GM12891	blood:	n/a
10	chr7:19453933-19453983	HL-60	blood:	n/a
11	chr7:19443825-19443875	GM12891	blood:	n/a
12	chr7:19408343-19408393	HCPEpiC	choroid plexus:	n/a
13	chr7:19408343-19408393	LNCaP	prostate:	n/a
14	chr7:19443825-19443875	BE2_C	brain:	n/a
15	chr7:19443825-19443875	MCF-7	breast:	n/a
16	chr7:19453933-19453983	SK-N-SH_RA	brain:	n/a
17	chr7:19443825-19443875	HEEpiC	esophagus:	n/a
18	chr7:19408343-19408393	GM12891	blood:	n/a
19	chr7:19443825-19443875	HCM	heart:	n/a
20	chr7:19453933-19453983	HRPEpiC	eye:	n/a
21	chr7:19408343-19408393	HRPEpiC	eye:	n/a
22	chr7:19417585-19417635	AG09319	gingival:	n/a
23	chr7:19443825-19443875	NB4	blood:	n/a
24	chr7:19408343-19408393	RPTEC	kidney:	n/a
25	chr7:19443825-19443875	AG09319	gingival:	n/a
26	chr7:19453933-19453983	AG04450	lung:	fetal
27	chr7:19443825-19443875	BJ	skin:	n/a
28	chr7:19453933-19453983	NH-A	brain:	n/a
29	chr7:19417585-19417635	NH-A	brain:	n/a
30	chr7:19443825-19443875	AG09309	skin:	n/a
31	chr7:19417585-19417635	GM06990	blood:	n/a
32	chr7:19417585-19417635	HNPCEpiC	eye:	n/a
33	chr7:19417585-19417635	PrEC	prostate:	n/a
34	chr7:19443825-19443875	GM12878	blood:	n/a
35	chr7:19408343-19408393	Hela-S3	cervix:	n/a
36	chr7:19417585-19417635	HIPEpiC	eye:	n/a
37	chr7:19417585-19417635	GM12892	blood:	n/a
38	chr7:19443825-19443875	NHDF-neo	bronchial:	n/a
39	chr7:19453933-19453983	MCF-7	breast:	n/a
40	chr7:19408343-19408393	AG09319	gingival:	n/a
41	chr7:19408343-19408393	SK-N-SH	brain:	n/a
42	chr7:19408343-19408393	SKMC	muscle:	n/a
43	chr7:19417585-19417635	MCF-7	breast:	n/a
44	chr7:19417585-19417635	NHBE	bronchial:	n/a
45	chr7:19408343-19408393	AoSMC	blood vessel:	n/a
46	chr7:19453933-19453983	AG09309	skin:	n/a
47	chr7:19453933-19453983	HEK293	kidney:	embryo
48	chr7:19453933-19453983	HUVEC	blood vessel:	n/a
49	chr7:19408343-19408393	HepG2	liver:	n/a
50	chr7:19408343-19408393	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:19429082..19431210-chr7:19440295..19442664,2	K562	blood:
2	chr7:19429082..19431210-chr7:19440295..19442664,2	K562	blood:
3	chr7:19400460..19402875-chr7:19412134..19413923,2	K562	blood:
4	chr7:19400460..19402875-chr7:19412134..19413923,2	K562	blood:
5	chr7:19161356..19162289-chr7:19481424..19482541,6	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HDAC9-5	chr7:19443324-19443386	ENSG00000223838
2	lnc-HDAC9-5	chr7:19393157-19393264	ENSG00000223838
3	lnc-HDAC9-12	chr7:19409849-19409911	NONHSAT119386
4	lnc-HDAC9-5	chr7:19394363-19394508	ENSG00000223838
5	lnc-HDAC9-5	chr7:19444955-19444993	ENSG00000223838
6	lnc-HDAC9-12	chr7:19411480-19411518	NONHSAT119386

No data

Variant related genes	Relation type
ENSG00000223838	TF binding region
ENSG00000223838	CpG island

Extended variants
information (count: 3724 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:3724 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116626648	chr7:19364028-19364029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555177699	chr7:19364041-19364042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368108491	chr7:19364057-19364058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147620587	chr7:19364101-19364102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140779215	chr7:19364133-19364134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563432435	chr7:19364181-19364182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183876113	chr7:19364199-19364200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546152940	chr7:19364204-19364205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370061944	chr7:19364225-19364226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77537865	chr7:19364240-19364241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs3028338	chr7:19364241-19364242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs75326756	chr7:19364242-19364243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375399885	chr7:19364243-19364244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76173270	chr7:19364244-19364245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs5882701	chr7:19364246-19364247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9918502	chr7:19364248-19364249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560695834	chr7:19364250-19364251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs71017036	chr7:19364266-19364267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376150737	chr7:19364275-19364276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185070913	chr7:19364289-19364290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560882011	chr7:19364293-19364294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs16872218	chr7:19364294-19364295	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs546433387	chr7:19364296-19364297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113294241	chr7:19364339-19364340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566539837	chr7:19364351-19364352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190222374	chr7:19364371-19364372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs17352934	chr7:19364385-19364386	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs529501960	chr7:19364387-19364388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551938108	chr7:19364456-19364457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181726801	chr7:19364457-19364458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568885556	chr7:19364546-19364547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539081986	chr7:19364597-19364598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1860800	chr7:19364625-19364626	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs566328846	chr7:19364689-19364690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534122660	chr7:19364709-19364710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555239021	chr7:19364711-19364712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375259078	chr7:19364740-19364741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140928292	chr7:19364749-19364750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372345043	chr7:19364789-19364790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531197213	chr7:19364791-19364792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs56162247	chr7:19364893-19364894	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs186331388	chr7:19364902-19364903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371939498	chr7:19364948-19364949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564535742	chr7:19364959-19364960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6944896	chr7:19364985-19364986	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs540969704	chr7:19364997-19364998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562331206	chr7:19365015-19365016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529511857	chr7:19365019-19365020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551166422	chr7:19365023-19365024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562456964	chr7:19365025-19365026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:477 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:19357600-19366600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr7:19362000-19365800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:19362200-19366800	Weak transcription	Osteobl	bone
4	chr7:19365800-19368000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:19366400-19367000	Enhancers	HUVEC	blood vessel
6	chr7:19366600-19367200	Enhancers	Muscle Satellite Cultured Cells	--
7	chr7:19366600-19367200	Enhancers	Brain Angular Gyrus	brain
8	chr7:19366600-19367600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr7:19366600-19367800	Enhancers	Brain Substantia Nigra	brain
10	chr7:19366600-19369200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr7:19366800-19367200	Enhancers	Osteobl	bone
12	chr7:19366800-19368400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:19366800-19368400	Enhancers	Brain Hippocampus Middle	brain
14	chr7:19367000-19368000	Enhancers	Fetal Lung	lung
15	chr7:19367000-19368200	Enhancers	Brain Cingulate Gyrus	brain
16	chr7:19367200-19374200	Weak transcription	Brain Angular Gyrus	brain
17	chr7:19367800-19373000	Weak transcription	Brain Substantia Nigra	brain
18	chr7:19368000-19373200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:19368200-19372600	Weak transcription	Brain Cingulate Gyrus	brain
20	chr7:19368400-19372800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:19368400-19373400	Weak transcription	Brain Hippocampus Middle	brain
22	chr7:19372600-19373800	Enhancers	Brain Cingulate Gyrus	brain
23	chr7:19372800-19373400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr7:19373000-19373400	Enhancers	Brain Substantia Nigra	brain
25	chr7:19373200-19373800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr7:19373400-19373600	Enhancers	Brain Hippocampus Middle	brain
27	chr7:19373400-19373600	Weak transcription	Brain Substantia Nigra	brain
28	chr7:19373600-19374000	Enhancers	Brain Substantia Nigra	brain
29	chr7:19373800-19376600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr7:19374200-19374400	Enhancers	Brain Angular Gyrus	brain
31	chr7:19376600-19377000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr7:19377000-19378800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr7:19378800-19379200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr7:19378800-19380400	Enhancers	Placenta	Placenta
35	chr7:19380000-19380400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr7:19391000-19393400	Enhancers	NHDF-Ad	bronchial
37	chr7:19391200-19391800	Enhancers	Dnd41	blood
38	chr7:19391400-19392200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr7:19391600-19392000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr7:19391600-19392800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr7:19391600-19393200	Enhancers	HSMM	muscle
42	chr7:19391600-19393600	Enhancers	Osteobl	bone
43	chr7:19391800-19393200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr7:19391800-19393400	Enhancers	Muscle Satellite Cultured Cells	--
45	chr7:19392000-19393000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr7:19392200-19393400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr7:19393000-19393800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr7:19393400-19394800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr7:19394000-19394400	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr7:19394000-19394800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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