Variant report

Variant	nsv525887
Chromosome Location	chr9:18778319-18791355
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	BHLHE40	chr9:18791280-18791295	K562	blood:	n/a	n/a
2	CEBPB	chr9:18785708-18785903	IMR90	lung:	n/a	chr9:18785873-18785884
3	CTCF	chr9:18791140-18791290	HVMF	connective:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
4	CTCF	chr9:18791180-18791330	A549	lung:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
5	CTCF	chr9:18791161-18791357	GM12892	blood:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
6	CTCF	chr9:18791098-18791454	H1-hESC	embryonic stem cell:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
7	CTCF	chr9:18791200-18791350	GM12872	blood:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
8	CTCF	chr9:18791162-18791386	HepG2	liver:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
9	CTCF	chr9:18791160-18791310	GM12870	blood:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
10	CTCF	chr9:18791200-18791350	HCM	heart:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
11	CTCF	chr9:18791180-18791330	BE2_C	brain:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
12	CTCF	chr9:18791080-18791230	NHEK	skin:	n/a	n/a
13	CTCF	chr9:18791200-18791350	WERI-Rb-1	eye:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
14	CTCF	chr9:18791165-18791342	A549	lung:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
15	CTCF	chr9:18791220-18791370	HAc	cerebellar:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
16	CTCF	chr9:18791200-18791350	GM12864	blood:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
17	CTCF	chr9:18791240-18791390	HCT-116	colon:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
18	CTCF	chr9:18791173-18791381	MCF-7	breast:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
19	CTCF	chr9:18791200-18791350	HMEC	breast:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
20	CTCF	chr9:18791174-18791366	SK-N-SH_RA	brain:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
21	CTCF	chr9:18791056-18791441	H1-hESC	embryonic stem cell:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
22	CTCF	chr9:18791180-18791330	GM12867	blood:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
23	CTCF	chr9:18791200-18791350	GM12865	blood:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
24	CTCF	chr9:18791220-18791370	HRPEpiC	eye:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
25	CTCF	chr9:18791180-18791330	HPF	lung:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
26	CTCF	chr9:18791185-18791378	Gliobla	brain:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
27	CTCF	chr9:18791180-18791330	HEEpiC	esophagus:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
28	CTCF	chr9:18791079-18791458	K562	blood:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
29	CTCF	chr9:18791200-18791350	BE2_C	brain:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
30	CTCF	chr9:18791200-18791350	K562	blood:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
31	CTCF	chr9:18791182-18791404	LNCaP	prostate:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
32	CTCF	chr9:18791160-18791310	HEEpiC	esophagus:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
33	CTCF	chr9:18791153-18791356	MCF-7	breast:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
34	CTCF	chr9:18791200-18791350	HRPEpiC	eye:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
35	CTCF	chr9:18791220-18791370	HCPEpiC	choroid plexus:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
36	CTCF	chr9:18791260-18791410	GM12867	blood:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
37	CTCF	chr9:18791160-18791310	GM12864	blood:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
38	CTCF	chr9:18791117-18791389	K562	blood:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
39	CTCF	chr9:18791140-18791290	GM12875	blood:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
40	CTCF	chr9:18791200-18791350	HBMEC	blood vessel:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
41	CTCF	chr9:18791220-18791370	GM12868	blood:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
42	CTCF	chr9:18791200-18791350	HCPEpiC	choroid plexus:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
43	CTCF	chr9:18791160-18791310	GM12875	blood:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
44	CTCF	chr9:18791180-18791330	RPTEC	kidney:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
45	CTCF	chr9:18791180-18791330	SAEC	small airway:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
46	CTCF	chr9:18791107-18791492	HepG2	liver:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
47	CTCF	chr9:18791220-18791370	HMEC	breast:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
48	CTCF	chr9:18791200-18791350	GM12873	blood:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285
49	CTCF	chr9:18791080-18791230	GM12869	blood:	n/a	n/a
50	CTCF	chr9:18791140-18791290	HAc	cerebellar:	n/a	chr9:18791268-18791284 chr9:18791269-18791282 chr9:18791267-18791285

No.	Distal block	Cell Line	Cell type
1	chr9:18254776..18255758-chr9:18790832..18791755,3	MCF-7	breast:
2	chr9:18777312..18778984-chr9:18781193..18784128,2	K562	blood:
3	chr9:18769799..18772875-chr9:18776003..18779587,3	K562	blood:
4	chr9:18791200..18791746-chr9:19457106..19458088,3	K562	blood:
5	chr9:18777312..18778984-chr9:18781193..18784128,2	K562	blood:
6	chr9:18770497..18772251-chr9:18783540..18785289,2	K562	blood:

Variant related genes	Relation type
ADAMTSL1	TF binding region

Extended variants
information (count: 584 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2289006	chr9:18778319-18778320	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575662046	chr9:18778326-18778327	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs117551426	chr9:18778338-18778339	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564249775	chr9:18778385-18778386	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528339633	chr9:18778396-18778397	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190431074	chr9:18778441-18778442	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs148756532	chr9:18778492-18778493	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs116494995	chr9:18778556-18778557	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs7038190	chr9:18778574-18778575	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs568901144	chr9:18778584-18778585	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs532871555	chr9:18778606-18778607	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs534584232	chr9:18778662-18778663	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs72690544	chr9:18778692-18778693	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs11791705	chr9:18778723-18778724	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs534896508	chr9:18778737-18778738	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs553202929	chr9:18778754-18778755	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs568680845	chr9:18778796-18778797	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs141456813	chr9:18778804-18778805	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs542389310	chr9:18778843-18778844	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs575619926	chr9:18778870-18778871	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs11789625	chr9:18778885-18778886	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs150834513	chr9:18778914-18778915	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs573035444	chr9:18778933-18778934	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs540434488	chr9:18778945-18778946	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs139236586	chr9:18778962-18778963	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs144162830	chr9:18778982-18778983	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs146016613	chr9:18779003-18779004	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs562324811	chr9:18779034-18779035	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs113497459	chr9:18779056-18779057	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs182691714	chr9:18779092-18779093	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs56016185	chr9:18779129-18779130	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs187400749	chr9:18779130-18779131	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs546804829	chr9:18779159-18779160	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs568669911	chr9:18779175-18779176	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs535749600	chr9:18779230-18779231	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs543810621	chr9:18779234-18779235	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs139922863	chr9:18779248-18779249	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs571865463	chr9:18779285-18779286	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs74565851	chr9:18779355-18779356	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs73644665	chr9:18779364-18779365	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs562609347	chr9:18779394-18779395	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs192246677	chr9:18779397-18779398	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs73419065	chr9:18779428-18779429	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs555256378	chr9:18779434-18779435	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs112535160	chr9:18779448-18779449	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs564496435	chr9:18779460-18779461	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs1347266	chr9:18779480-18779481	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs143419023	chr9:18779495-18779496	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs373874562	chr9:18779497-18779498	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs6475245	chr9:18779520-18779521	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:86)

Disease	PMID	Source
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Myelofibrosis	22110671	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:169 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18748200-18779600	Weak transcription	Colonic Mucosa	Colon
2	chr9:18756800-18787200	Weak transcription	HSMMtube	muscle
3	chr9:18764000-18781000	Strong transcription	Osteobl	bone
4	chr9:18768800-18780200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr9:18769200-18780200	Strong transcription	NH-A	brain
6	chr9:18771000-18781600	Strong transcription	Muscle Satellite Cultured Cells	--
7	chr9:18772200-18785600	Weak transcription	Colon Smooth Muscle	Colon
8	chr9:18772800-18781000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr9:18773000-18786200	Weak transcription	Right Ventricle	heart
10	chr9:18775800-18778400	Enhancers	Pancreas	Pancrea
11	chr9:18775800-18780200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr9:18776400-18778600	Strong transcription	NHLF	lung
13	chr9:18776400-18778800	Weak transcription	Fetal Brain Female	brain
14	chr9:18776400-18786200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr9:18777000-18778400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr9:18777000-18778600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr9:18777000-18784000	Weak transcription	Adipose Nuclei	Adipose
18	chr9:18777200-18786400	Weak transcription	Fetal Intestine Small	intestine
19	chr9:18777600-18778800	Weak transcription	Brain Germinal Matrix	brain
20	chr9:18777600-18779600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr9:18777600-18779600	Strong transcription	NHDF-Ad	bronchial
22	chr9:18777600-18779800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr9:18777800-18778400	Genic enhancers	Fetal Muscle Leg	muscle
24	chr9:18777800-18778400	Genic enhancers	Fetal Stomach	stomach
25	chr9:18777800-18780400	Weak transcription	Gastric	stomach
26	chr9:18777800-18780600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr9:18777800-18786200	Strong transcription	HSMM	muscle
28	chr9:18778000-18778400	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr9:18778000-18778400	Enhancers	Fetal Muscle Trunk	muscle
30	chr9:18778000-18779400	Enhancers	Fetal Heart	heart
31	chr9:18778000-18782600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr9:18778000-18798200	Weak transcription	Aorta	Aorta
33	chr9:18778200-18778800	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr9:18778200-18779600	Enhancers	HUVEC	blood vessel
35	chr9:18778200-18779800	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr9:18778400-18778600	Enhancers	Fetal Kidney	kidney
37	chr9:18778400-18779400	Weak transcription	Fetal Muscle Trunk	muscle
38	chr9:18778400-18779400	Weak transcription	Fetal Stomach	stomach
39	chr9:18778400-18786000	Weak transcription	Fetal Muscle Leg	muscle
40	chr9:18778400-18817000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr9:18778600-18779400	Weak transcription	Fetal Kidney	kidney
42	chr9:18778600-18785800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr9:18778600-18796000	Weak transcription	NHLF	lung
44	chr9:18778800-18779200	Enhancers	Brain Germinal Matrix	brain
45	chr9:18779400-18779600	Enhancers	Fetal Kidney	kidney
46	chr9:18779400-18779800	Enhancers	Fetal Muscle Trunk	muscle
47	chr9:18779400-18780200	Strong transcription	Fetal Stomach	stomach
48	chr9:18779400-18785200	Weak transcription	Fetal Heart	heart
49	chr9:18779600-18781200	Weak transcription	HUVEC	blood vessel
50	chr9:18779600-18781800	Weak transcription	NHDF-Ad	bronchial

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