Variant report

Variant	nsv465743
Chromosome Location	chr8:96472423-96518204
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	BATF	chr8:96480282-96480525	GM12878	blood:	n/a	n/a
2	BHLHE40	chr8:96481569-96481741	GM12878	blood:	n/a	n/a
3	CBX3	chr8:96478360-96478944	HCT-116	colon:	n/a	n/a
4	CBX3	chr8:96478331-96478912	HCT-116	colon:	n/a	n/a
5	CEBPB	chr8:96484840-96485017	H1-hESC	embryonic stem cell:	n/a	chr8:96484909-96484926
6	CEBPB	chr8:96484759-96485089	IMR90	lung:	n/a	chr8:96484909-96484926
7	CEBPB	chr8:96478325-96478326	K562	blood:	n/a	n/a
8	CEBPB	chr8:96478191-96478453	HepG2	liver:	n/a	chr8:96478350-96478361
9	CEBPB	chr8:96474317-96474538	HepG2	liver:	n/a	n/a
10	CTCF	chr8:96515803-96515868	GM12878	blood:	n/a	chr8:96515820-96515833
11	CTCF	chr8:96515731-96515906	MCF-7	breast:	n/a	chr8:96515820-96515833
12	CTCF	chr8:96515720-96515870	HMEC	breast:	n/a	chr8:96515820-96515833
13	CTCF	chr8:96515653-96515968	H1-hESC	embryonic stem cell:	n/a	chr8:96515820-96515833
14	CTCF	chr8:96483447-96483507	GM20000	blood:	n/a	n/a
15	CTCF	chr8:96515723-96515934	Fibrobl	skin:	n/a	chr8:96515820-96515833
16	CTCF	chr8:96515760-96515910	AG10803	skin:	n/a	chr8:96515820-96515833
17	CTCF	chr8:96515660-96515810	HCM	heart:	n/a	n/a
18	CTCF	chr8:96515720-96515870	NHDF-neo	bronchial:	n/a	chr8:96515820-96515833
19	CTCF	chr8:96515760-96515910	HCPEpiC	choroid plexus:	n/a	chr8:96515820-96515833
20	CTCF	chr8:96515740-96515890	HEEpiC	esophagus:	n/a	chr8:96515820-96515833
21	CTCF	chr8:96515553-96516093	MCF-7	breast:	n/a	chr8:96515820-96515833
22	CTCF	chr8:96515719-96515925	MCF-7	breast:	n/a	chr8:96515820-96515833
23	CTCF	chr8:96515780-96515930	HRE	kidney:	n/a	chr8:96515820-96515833
24	CTCF	chr8:96515780-96515930	RPTEC	kidney:	n/a	chr8:96515820-96515833
25	CTCF	chr8:96515746-96515892	LNCaP	prostate:	n/a	chr8:96515820-96515833
26	CTCF	chr8:96515777-96515895	MCF-7	breast:	n/a	chr8:96515820-96515833
27	CTCF	chr8:96515720-96515870	AoAF	blood vessel:	n/a	chr8:96515820-96515833
28	CTCF	chr8:96515880-96516030	HCM	heart:	n/a	n/a
29	CTCF	chr8:96515760-96515910	AG09309	skin:	n/a	chr8:96515820-96515833
30	CTCF	chr8:96515740-96515890	AG04449	skin:	n/a	chr8:96515820-96515833
31	CTCF	chr8:96515700-96515850	HMEC	breast:	n/a	chr8:96515820-96515833
32	CTCF	chr8:96515780-96515930	GM06990	blood:	n/a	chr8:96515820-96515833
33	CTCF	chr8:96515692-96515957	K562	blood:	n/a	chr8:96515820-96515833
34	CTCF	chr8:96515720-96515870	WI-38	lung:	n/a	chr8:96515820-96515833
35	CTCF	chr8:96515760-96515910	MCF-7	breast:	n/a	chr8:96515820-96515833
36	CTCF	chr8:96515568-96516050	HCT-116	colon:	n/a	chr8:96515820-96515833
37	CTCF	chr8:96515720-96515870	NHLF	lung:	n/a	chr8:96515820-96515833
38	CTCF	chr8:96515755-96515908	A549	lung:	n/a	chr8:96515820-96515833
39	CTCF	chr8:96515720-96515870	AG09319	gingival:	n/a	chr8:96515820-96515833
40	CTCF	chr8:96515695-96515954	Gliobla	brain:	n/a	chr8:96515820-96515833
41	CTCF	chr8:96515740-96515890	NHDF-neo	bronchial:	n/a	chr8:96515820-96515833
42	CTCF	chr8:96493940-96494090	AG04449	skin:	n/a	chr8:96494027-96494040
43	CTCF	chr8:96515700-96515850	Caco-2	colon:	n/a	chr8:96515820-96515833
44	CTCF	chr8:96515806-96515837	GM19238	blood:	n/a	chr8:96515820-96515833
45	CTCF	chr8:96515707-96515921	ProgFib	skin:	n/a	chr8:96515820-96515833
46	CTCF	chr8:96515760-96515910	A549	lung:	n/a	chr8:96515820-96515833
47	CTCF	chr8:96515740-96515890	HA-sp	spinal cord:	n/a	chr8:96515820-96515833
48	CTCF	chr8:96515720-96515870	HAc	cerebellar:	n/a	chr8:96515820-96515833
49	CTCF	chr8:96515760-96515910	AoAF	blood vessel:	n/a	chr8:96515820-96515833
50	CTCF	chr8:96515740-96515890	HCPEpiC	choroid plexus:	n/a	chr8:96515820-96515833

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:96504381-96504431	HNPCEpiC	eye:	n/a
2	chr8:96504381-96504431	AG10803	skin:	n/a
3	chr8:96504381-96504431	HL-60	blood:	n/a
4	chr8:96497618-96497668	HRCEpiC	kidney:	n/a
5	chr8:96504381-96504431	Hela-S3	cervix:	n/a
6	chr8:96497618-96497668	K562	blood:	n/a
7	chr8:96497618-96497668	AG04449	skin:	fetal
8	chr8:96504381-96504431	GM12878	blood:	n/a
9	chr8:96504381-96504431	HCM	heart:	n/a
10	chr8:96504381-96504431	ECC-1	luminal epithelium:	n/a
11	chr8:96497618-96497668	Caco-2	colon:	n/a
12	chr8:96497618-96497668	HEEpiC	esophagus:	n/a
13	chr8:96504381-96504431	PrEC	prostate:	n/a
14	chr8:96504381-96504431	HCF	heart:	n/a
15	chr8:96497618-96497668	A549	lung:	n/a
16	chr8:96504381-96504431	AG04450	lung:	fetal
17	chr8:96497618-96497668	HPAEpiC	pulmonary alveolar:	n/a
18	chr8:96497618-96497668	ECC-1	luminal epithelium:	n/a
19	chr8:96504381-96504431	SAEC	small airway:	n/a
20	chr8:96497618-96497668	AoSMC	blood vessel:	n/a
21	chr8:96504381-96504431	ProgFib	skin:	n/a
22	chr8:96497618-96497668	PrEC	prostate:	n/a
23	chr8:96504381-96504431	AG09309	skin:	n/a
24	chr8:96504381-96504431	HRCEpiC	kidney:	n/a
25	chr8:96504381-96504431	Jurkat	blood:	n/a
26	chr8:96497618-96497668	AG09309	skin:	n/a
27	chr8:96497618-96497668	GM12892	blood:	n/a
28	chr8:96504381-96504431	PFSK-1	brain:	n/a
29	chr8:96497618-96497668	BE2_C	brain:	n/a
30	chr8:96497618-96497668	SKMC	muscle:	n/a
31	chr8:96497618-96497668	AG09319	gingival:	n/a
32	chr8:96504381-96504431	HCT-116	colon:	n/a
33	chr8:96497618-96497668	HRE	kidney:	n/a
34	chr8:96497618-96497668	Hela-S3	cervix:	n/a
35	chr8:96497618-96497668	AG04450	lung:	fetal
36	chr8:96504381-96504431	Caco-2	colon:	n/a
37	chr8:96497618-96497668	SK-N-MC	brain:	n/a
38	chr8:96497618-96497668	HAEpiC	amniotic membrane:	n/a
39	chr8:96504381-96504431	Hepatocyte	liver:	n/a
40	chr8:96497618-96497668	Jurkat	blood:	n/a
41	chr8:96497618-96497668	HCPEpiC	choroid plexus:	n/a
42	chr8:96497618-96497668	T-47D	breast:	n/a
43	chr8:96497618-96497668	LNCaP	prostate:	n/a
44	chr8:96497618-96497668	HCM	heart:	n/a
45	chr8:96497618-96497668	GM06990	blood:	n/a
46	chr8:96497618-96497668	HL-60	blood:	n/a
47	chr8:96504381-96504431	HRE	kidney:	n/a
48	chr8:96497618-96497668	GM12891	blood:	n/a
49	chr8:96497618-96497668	ProgFib	skin:	n/a
50	chr8:96497618-96497668	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:96515360..96516198-chr8:96770656..96771587,2	MCF-7	breast:
2	chr8:96495853..96497993-chr8:96501094..96502749,2	K562	blood:
3	chr8:96480054..96482091-chr8:96490251..96491992,2	K562	blood:
4	chr8:96475186..96478156-chr8:96479951..96482141,2	K562	blood:
5	chr8:96475186..96478156-chr8:96479951..96482141,2	K562	blood:
6	chr8:96466484..96468779-chr8:96473364..96475271,2	K562	blood:
7	chr8:96475902..96478183-chr8:96480262..96482301,2	K562	blood:
8	chr8:96480054..96482091-chr8:96490251..96491992,2	K562	blood:
9	chr13:83085927..83086427-chr8:96515336..96516158,2	MCF-7	breast:
10	chr8:96475902..96478183-chr8:96480262..96482301,2	K562	blood:
11	chr3:40507548..40508387-chr8:96488685..96489340,2	MCF-7	breast:
12	chr8:96495853..96497993-chr8:96501094..96502749,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLEKHF2-1	chr8:96517634-96517853	ENSG00000253872

Variant related genes	Relation type
ENSG00000253872	TF binding region
ENSG00000253872	CpG island
ENSG00000272452	chromatin interactions

Extended variants
information (count: 1268 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:1268 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7835982	chr8:96472423-96472424	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147322671	chr8:96472454-96472455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184409975	chr8:96472491-96472492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs3133787	chr8:96472512-96472513	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs147993070	chr8:96472599-96472600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188170140	chr8:96472630-96472631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575029602	chr8:96472671-96472672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs75468103	chr8:96472743-96472744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74361892	chr8:96472746-96472747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558116266	chr8:96472764-96472765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181929052	chr8:96472789-96472790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs3133788	chr8:96472820-96472821	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs3104926	chr8:96472838-96472839	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs111354478	chr8:96472861-96472862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560774228	chr8:96472885-96472886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574057034	chr8:96472888-96472889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543062051	chr8:96472892-96472893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7836474	chr8:96472930-96472931	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs6986230	chr8:96472936-96472937	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs3968025	chr8:96472965-96472966	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs570726567	chr8:96472969-96472970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs11986277	chr8:96472997-96472998	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs186298946	chr8:96473011-96473012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536437505	chr8:96473019-96473020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189423144	chr8:96473041-96473042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6987556	chr8:96473042-96473043	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs4404882	chr8:96473087-96473088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376430959	chr8:96473102-96473103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369967475	chr8:96473111-96473112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6987593	chr8:96473121-96473122	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs548113398	chr8:96473163-96473164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75514223	chr8:96473164-96473165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186870841	chr8:96473199-96473200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373465575	chr8:96473219-96473220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573332451	chr8:96473227-96473228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535568734	chr8:96473315-96473316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557844036	chr8:96473319-96473320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4320522	chr8:96473324-96473325	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs534419124	chr8:96473336-96473337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs3104927	chr8:96473354-96473355	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs574422221	chr8:96473379-96473380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543023278	chr8:96473388-96473389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs4295633	chr8:96473417-96473418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556634130	chr8:96473422-96473423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7840782	chr8:96473431-96473432	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs55642149	chr8:96473433-96473434	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs146518545	chr8:96473434-96473435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532949034	chr8:96473546-96473547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540070701	chr8:96473573-96473574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs16917722	chr8:96473610-96473611	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Malignant melanoma	17260012	CNVD

Chromatin state (count:143 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96470600-96474800	Weak transcription	Left Ventricle	heart
2	chr8:96472000-96472800	Enhancers	H9 Cell Line	embryonic stem cell
3	chr8:96472000-96478600	Weak transcription	Aorta	Aorta
4	chr8:96477400-96477600	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr8:96478000-96478800	Enhancers	HUVEC	blood vessel
6	chr8:96478600-96478800	ZNF genes & repeats	Aorta	Aorta
7	chr8:96478800-96481200	Weak transcription	Aorta	Aorta
8	chr8:96478800-96482200	Weak transcription	HUVEC	blood vessel
9	chr8:96482200-96483200	Enhancers	HUVEC	blood vessel
10	chr8:96482200-96483600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:96483600-96485800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:96485800-96486200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:96492600-96493200	Enhancers	Pancreas	Pancrea
14	chr8:96492800-96494200	Enhancers	Colon Smooth Muscle	Colon
15	chr8:96493000-96494200	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr8:96493200-96493600	Weak transcription	Pancreas	Pancrea
17	chr8:96493200-96493600	Enhancers	Stomach Smooth Muscle	stomach
18	chr8:96493200-96493800	Enhancers	Fetal Muscle Leg	muscle
19	chr8:96493200-96494000	Enhancers	Fetal Stomach	stomach
20	chr8:96493200-96494200	Enhancers	Fetal Lung	lung
21	chr8:96493200-96494400	Enhancers	Fetal Heart	heart
22	chr8:96493400-96493800	Bivalent Enhancer	Fetal Brain Male	brain
23	chr8:96493400-96494000	Enhancers	Fetal Brain Female	brain
24	chr8:96493400-96494000	Enhancers	Right Ventricle	heart
25	chr8:96493400-96494200	Enhancers	Ovary	ovary
26	chr8:96493400-96494400	Enhancers	Rectal Smooth Muscle	rectum
27	chr8:96493600-96493800	Flanking Active TSS	Stomach Smooth Muscle	stomach
28	chr8:96493600-96494000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr8:96493600-96494000	Enhancers	Brain Germinal Matrix	brain
30	chr8:96493600-96494000	Enhancers	Psoas Muscle	Psoas
31	chr8:96493600-96494000	Enhancers	HSMMtube	muscle
32	chr8:96493600-96494200	Enhancers	Brain Substantia Nigra	brain
33	chr8:96493600-96494200	Enhancers	Pancreas	Pancrea
34	chr8:96493600-96494400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr8:96493600-96494400	Enhancers	Adipose Nuclei	Adipose
36	chr8:96493600-96494600	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr8:96493800-96494000	Enhancers	Osteobl	bone
38	chr8:96493800-96494200	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr8:96493800-96494200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr8:96493800-96494200	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr8:96493800-96494200	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr8:96493800-96497400	Weak transcription	Stomach Smooth Muscle	stomach
43	chr8:96494000-96494200	Enhancers	HSMM	muscle
44	chr8:96494000-96497200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr8:96494000-96497200	Weak transcription	HSMMtube	muscle
46	chr8:96494200-96497000	Weak transcription	Colon Smooth Muscle	Colon
47	chr8:96494200-96497400	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr8:96494400-96496800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr8:96494400-96497000	Weak transcription	Osteobl	bone
50	chr8:96494400-96497400	Weak transcription	Fetal Heart	heart

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