Variant report

Variant	nsv523497
Chromosome Location	chr7:18896011-18959381
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	ATF2	chr7:18906219-18906620	GM12878	blood:	n/a	n/a
2	ATF2	chr7:18906223-18906663	GM12878	blood:	n/a	n/a
3	BATF	chr7:18906302-18906552	GM12878	blood:	n/a	chr7:18906452-18906462
4	BATF	chr7:18901069-18901384	GM12878	blood:	n/a	n/a
5	BATF	chr7:18901100-18901360	GM12878	blood:	n/a	n/a
6	BATF	chr7:18906275-18906574	GM12878	blood:	n/a	chr7:18906452-18906462
7	BCL11A	chr7:18901144-18901466	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:18906200-18906608	GM12878	blood:	n/a	n/a
9	BCL3	chr7:18906281-18906582	GM12878	blood:	n/a	n/a
10	BCL3	chr7:18901075-18901327	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:18906266-18906637	GM12878	blood:	n/a	n/a
12	CBX3	chr7:18906155-18906611	HCT-116	colon:	n/a	n/a
13	CBX3	chr7:18934946-18935470	HCT-116	colon:	n/a	n/a
14	CEBPB	chr7:18906077-18906670	Hela-S3	cervix:	n/a	chr7:18906311-18906324
15	CEBPB	chr7:18897769-18897962	HepG2	liver:	n/a	chr7:18897821-18897833
16	CEBPB	chr7:18901148-18901407	A549	lung:	n/a	chr7:18901252-18901263 chr7:18901252-18901265 chr7:18901253-18901264
17	CEBPB	chr7:18897174-18897363	A549	lung:	n/a	n/a
18	CEBPB	chr7:18900339-18900583	HepG2	liver:	n/a	chr7:18900431-18900442 chr7:18900430-18900441
19	CEBPB	chr7:18899029-18899282	HepG2	liver:	n/a	n/a
20	CEBPB	chr7:18897635-18897925	IMR90	lung:	n/a	chr7:18897821-18897833
21	CEBPB	chr7:18901118-18901398	HepG2	liver:	n/a	chr7:18901252-18901263 chr7:18901252-18901265 chr7:18901253-18901264
22	CEBPB	chr7:18904425-18904502	K562	blood:	n/a	chr7:18904458-18904469
23	CEBPB	chr7:18901060-18901509	IMR90	lung:	n/a	chr7:18901252-18901263 chr7:18901252-18901265 chr7:18901253-18901264
24	CEBPB	chr7:18905971-18906708	IMR90	lung:	n/a	chr7:18906311-18906324
25	CEBPB	chr7:18934830-18935687	HCT-116	colon:	n/a	chr7:18935614-18935626
26	CEBPB	chr7:18940561-18940789	IMR90	lung:	n/a	chr7:18940689-18940702 chr7:18940622-18940635
27	CEBPB	chr7:18904351-18904623	HepG2	liver:	n/a	chr7:18904458-18904469
28	CEBPB	chr7:18900297-18900566	IMR90	lung:	n/a	chr7:18900431-18900442 chr7:18900430-18900441
29	CEBPB	chr7:18904324-18904503	A549	lung:	n/a	chr7:18904458-18904469
30	CEBPB	chr7:18945099-18945329	A549	lung:	n/a	n/a
31	CHD2	chr7:18906355-18906585	GM12878	blood:	n/a	n/a
32	CREB1	chr7:18906153-18906647	GM12878	blood:	n/a	n/a
33	CTCF	chr7:18946640-18946790	SK-N-SH_RA	brain:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
34	CTCF	chr7:18913440-18913590	HPAF	blood vessel:	n/a	chr7:18913473-18913482 chr7:18913470-18913488 chr7:18913472-18913493
35	CTCF	chr7:18913440-18913590	HCM	heart:	n/a	chr7:18913473-18913482 chr7:18913470-18913488 chr7:18913472-18913493
36	CTCF	chr7:18913361-18913602	Fibrobl	skin:	n/a	chr7:18913473-18913482 chr7:18913470-18913488 chr7:18913472-18913493
37	CTCF	chr7:18913460-18913610	NB4	blood:	n/a	chr7:18913473-18913482 chr7:18913470-18913488 chr7:18913472-18913493
38	CTCF	chr7:18913360-18913510	WI-38	lung:	n/a	chr7:18913473-18913482 chr7:18913470-18913488 chr7:18913472-18913493
39	CTCF	chr7:18932780-18932930	HEK293	kidney:	n/a	n/a
40	CTCF	chr7:18946600-18946750	HRPEpiC	eye:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
41	CTCF	chr7:18933956-18933988	Medullo	brain:	n/a	n/a
42	CTCF	chr7:18946660-18946810	HCT-116	colon:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
43	CTCF	chr7:18946675-18946756	Fibrobl	skin:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
44	CTCF	chr7:18913420-18913570	HA-sp	spinal cord:	n/a	chr7:18913473-18913482 chr7:18913470-18913488 chr7:18913472-18913493
45	CTCF	chr7:18930720-18930870	BE2_C	brain:	n/a	n/a
46	CTCF	chr7:18946654-18946790	HUVEC	blood vessel:	n/a	chr7:18946706-18946724 chr7:18946708-18946729 chr7:18946707-18946723 chr7:18946709-18946722
47	CTCF	chr7:18913360-18913510	GM12865	blood:	n/a	chr7:18913473-18913482 chr7:18913470-18913488 chr7:18913472-18913493
48	CTCF	chr7:18913400-18913550	HRE	kidney:	n/a	chr7:18913473-18913482 chr7:18913470-18913488 chr7:18913472-18913493
49	CTCF	chr7:18913380-18913530	HAc	cerebellar:	n/a	chr7:18913473-18913482 chr7:18913470-18913488 chr7:18913472-18913493
50	CTCF	chr7:18913380-18913530	SAEC	small airway:	n/a	chr7:18913473-18913482 chr7:18913470-18913488 chr7:18913472-18913493

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:18929612-18929662	HCPEpiC	choroid plexus:	n/a
2	chr7:18929612-18929662	SKMC	muscle:	n/a
3	chr7:18929612-18929662	HNPCEpiC	eye:	n/a
4	chr7:18929612-18929662	Hepatocyte	liver:	n/a
5	chr7:18929612-18929662	HCF	heart:	n/a
6	chr7:18906433-18906483	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:18929612-18929662	HepG2	liver:	n/a
8	chr7:18929612-18929662	K562	blood:	n/a
9	chr7:18906433-18906483	GM12892	blood:	n/a
10	chr7:18906433-18906483	AG04449	skin:	fetal
11	chr7:18929612-18929662	MCF-7	breast:	n/a
12	chr7:18906433-18906483	NT2-D1	testis:	n/a
13	chr7:18929612-18929662	SK-N-MC	brain:	n/a
14	chr7:18906433-18906483	LNCaP	prostate:	n/a
15	chr7:18906433-18906483	Jurkat	blood:	n/a
16	chr7:18929612-18929662	SAEC	small airway:	n/a
17	chr7:18929612-18929662	PrEC	prostate:	n/a
18	chr7:18929612-18929662	NB4	blood:	n/a
19	chr7:18929612-18929662	HMEC	breast:	n/a
20	chr7:18906433-18906483	HRCEpiC	kidney:	n/a
21	chr7:18906433-18906483	HCF	heart:	n/a
22	chr7:18906433-18906483	HIPEpiC	eye:	n/a
23	chr7:18906433-18906483	HCPEpiC	choroid plexus:	n/a
24	chr7:18929612-18929662	Jurkat	blood:	n/a
25	chr7:18929612-18929662	GM12892	blood:	n/a
26	chr7:18906433-18906483	PANC-1	pancreas:	n/a
27	chr7:18929612-18929662	GM12878	blood:	n/a
28	chr7:18906433-18906483	IMR90	lung:	fetal
29	chr7:18929612-18929662	SK-N-SH_RA	brain:	n/a
30	chr7:18929612-18929662	AG09319	gingival:	n/a
31	chr7:18929612-18929662	NHBE	bronchial:	n/a
32	chr7:18906433-18906483	PFSK-1	brain:	n/a
33	chr7:18906433-18906483	NB4	blood:	n/a
34	chr7:18906433-18906483	AG09319	gingival:	n/a
35	chr7:18929612-18929662	HRPEpiC	eye:	n/a
36	chr7:18929612-18929662	HPAEpiC	pulmonary alveolar:	n/a
37	chr7:18906433-18906483	NH-A	brain:	n/a
38	chr7:18929612-18929662	AG04449	skin:	fetal
39	chr7:18929612-18929662	HIPEpiC	eye:	n/a
40	chr7:18929612-18929662	GM19239	blood:	n/a
41	chr7:18906433-18906483	T-47D	breast:	n/a
42	chr7:18929612-18929662	NT2-D1	testis:	n/a
43	chr7:18906433-18906483	K562	blood:	n/a
44	chr7:18929612-18929662	PANC-1	pancreas:	n/a
45	chr7:18906433-18906483	ECC-1	luminal epithelium:	n/a
46	chr7:18906433-18906483	GM19239	blood:	n/a
47	chr7:18906433-18906483	BJ	skin:	n/a
48	chr7:18929612-18929662	LNCaP	prostate:	n/a
49	chr7:18929612-18929662	AG09309	skin:	n/a
50	chr7:18906433-18906483	Hepatocyte	liver:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TWIST1-2	chr7:18932183-18932263	ENSG00000226522.1
2	lnc-TWIST1-2	chr7:18938932-18939056	ENSG00000226522.1
3	lnc-TWIST1-2	chr7:18931719-18931825	ENSG00000226522.1

Variant related genes	Relation type
ENSG00000226522	TF binding region
ENSG00000226522	CpG island

Extended variants
information (count: 2834 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2834 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2249817	chr7:18896011-18896012	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536986927	chr7:18896033-18896034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190558573	chr7:18896037-18896038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369457863	chr7:18896041-18896042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183806321	chr7:18896100-18896101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548580947	chr7:18896144-18896145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543015812	chr7:18896145-18896146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs75273105	chr7:18896186-18896187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144657320	chr7:18896187-18896188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377422020	chr7:18896264-18896265	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs540704701	chr7:18896269-18896270	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs559534571	chr7:18896334-18896335	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs553256888	chr7:18896340-18896341	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs3214116	chr7:18896381-18896382	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs397839905	chr7:18896388-18896389	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs187849805	chr7:18896394-18896395	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs116567212	chr7:18896407-18896408	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs566767689	chr7:18896420-18896421	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs563441647	chr7:18896423-18896424	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs538419664	chr7:18896435-18896436	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs148519772	chr7:18896436-18896437	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs550212207	chr7:18896445-18896446	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs567279233	chr7:18896467-18896468	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs571639114	chr7:18896471-18896472	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs532678733	chr7:18896536-18896537	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs142968927	chr7:18896557-18896558	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs151124965	chr7:18896584-18896585	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs536442827	chr7:18896595-18896596	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs367648727	chr7:18896643-18896644	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575225864	chr7:18896644-18896645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372205407	chr7:18896647-18896648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192957061	chr7:18896648-18896649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371124519	chr7:18896678-18896679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140895479	chr7:18896704-18896705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182359643	chr7:18896800-18896801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186687089	chr7:18896803-18896804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35048169	chr7:18896822-18896823	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs202202855	chr7:18896827-18896828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35041323	chr7:18896846-18896847	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs147934383	chr7:18896924-18896925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375575248	chr7:18896958-18896959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs60976379	chr7:18896959-18896960	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs397968923	chr7:18896987-18896988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377703827	chr7:18896988-18896989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373170975	chr7:18896992-18896993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73320014	chr7:18897003-18897004	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs77354398	chr7:18897006-18897007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545133367	chr7:18897038-18897039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76931863	chr7:18897039-18897040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546095148	chr7:18897059-18897060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18894600-18896200	Enhancers	NHDF-Ad	bronchial
2	chr7:18894600-18896600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr7:18895000-18896800	Enhancers	Osteobl	bone
4	chr7:18895400-18902800	Weak transcription	Aorta	Aorta
5	chr7:18895600-18896200	Enhancers	Muscle Satellite Cultured Cells	--
6	chr7:18895600-18897200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:18895800-18896400	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr7:18896200-18896600	Flanking Active TSS	NHDF-Ad	bronchial
9	chr7:18896200-18900800	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr7:18896600-18901800	Enhancers	NHDF-Ad	bronchial
11	chr7:18896800-18900600	Weak transcription	Osteobl	bone
12	chr7:18897200-18897600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr7:18897200-18900400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr7:18897600-18898600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:18898400-18899800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:18898400-18901800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr7:18898600-18899000	Enhancers	Primary T cells from cord blood	blood
18	chr7:18898600-18900400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:18900000-18900600	Enhancers	Fetal Stomach	stomach
20	chr7:18900000-18901600	Enhancers	Adipose Nuclei	Adipose
21	chr7:18900400-18900600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr7:18900400-18902400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:18900600-18901000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:18900600-18901800	Enhancers	Osteobl	bone
25	chr7:18900800-18901600	Enhancers	Muscle Satellite Cultured Cells	--
26	chr7:18901000-18901200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr7:18901000-18901600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr7:18901200-18901400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:18901400-18901800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr7:18901600-18904200	Weak transcription	Adipose Nuclei	Adipose
31	chr7:18901600-18905600	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr7:18901600-18905800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr7:18901800-18902000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:18901800-18905200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr7:18901800-18905200	Weak transcription	NHDF-Ad	bronchial
36	chr7:18901800-18905600	Weak transcription	Osteobl	bone
37	chr7:18902000-18904800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr7:18902400-18903800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr7:18902800-18903000	ZNF genes & repeats	Aorta	Aorta
40	chr7:18903000-18940000	Weak transcription	Aorta	Aorta
41	chr7:18903800-18907400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr7:18904200-18904400	Enhancers	Adipose Nuclei	Adipose
43	chr7:18904400-18904800	Weak transcription	Adipose Nuclei	Adipose
44	chr7:18904600-18906000	Enhancers	Right Atrium	heart
45	chr7:18904800-18907000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr7:18904800-18907400	Enhancers	Adipose Nuclei	Adipose
47	chr7:18905000-18907000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr7:18905200-18907000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr7:18905200-18908000	Enhancers	NHDF-Ad	bronchial
50	chr7:18905600-18906600	Enhancers	Muscle Satellite Cultured Cells	--

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