Variant report

Variant	nsv518975
Chromosome Location	chr8:94985722-94992958
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	chr8:94987380-94987732	K562	blood:	n/a	n/a
2	CTCF	chr8:94987500-94987650	GM12867	blood:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
3	CTCF	chr8:94987200-94987350	A549	lung:	n/a	n/a
4	CTCF	chr8:94987423-94987718	HUVEC	blood vessel:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
5	CTCF	chr8:94987480-94987630	HPAF	blood vessel:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
6	CTCF	chr8:94987480-94987630	GM12878	blood:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
7	CTCF	chr8:94987480-94987630	AG09309	skin:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
8	CTCF	chr8:94987500-94987650	GM12865	blood:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
9	CTCF	chr8:94987428-94987714	ProgFib	skin:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
10	CTCF	chr8:94987520-94987670	HRPEpiC	eye:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
11	CTCF	chr8:94987343-94987759	H1-hESC	embryonic stem cell:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
12	CTCF	chr8:94987480-94987630	AG04450	lung:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
13	CTCF	chr8:94987480-94987630	GM12871	blood:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
14	CTCF	chr8:94987419-94987719	NHEK	skin:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
15	CTCF	chr8:94987452-94987649	A549	lung:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
16	CTCF	chr8:94987500-94987650	HRE	kidney:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
17	CTCF	chr8:94987480-94987630	BE2_C	brain:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
18	CTCF	chr8:94987500-94987650	GM12875	blood:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
19	CTCF	chr8:94987500-94987650	GM12864	blood:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
20	CTCF	chr8:94987440-94987700	GM13977	blood:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
21	CTCF	chr8:94987520-94987670	A549	lung:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
22	CTCF	chr8:94987500-94987650	AoAF	blood vessel:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
23	CTCF	chr8:94987141-94987843	A549	lung:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
24	CTCF	chr8:94987500-94987650	RPTEC	kidney:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
25	CTCF	chr8:94987397-94987721	Medullo	brain:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
26	CTCF	chr8:94987407-94987670	A549	lung:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
27	CTCF	chr8:94987346-94987731	ECC-1	luminal epithelium:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
28	CTCF	chr8:94987500-94987650	HCM	heart:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
29	CTCF	chr8:94987238-94987915	MCF-7	breast:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
30	CTCF	chr8:94987283-94987846	MCF-7	breast:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
31	CTCF	chr8:94987480-94987630	GM12872	blood:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
32	CTCF	chr8:94987443-94987695	Hela-S3	cervix:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
33	CTCF	chr8:94987500-94987650	HMF	breast:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
34	CTCF	chr8:94987431-94987704	MCF-7	breast:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
35	CTCF	chr8:94987442-94987694	Pancreas_OC	pancreas:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
36	CTCF	chr8:94987420-94987570	HFF	foreskin:	n/a	n/a
37	CTCF	chr8:94987480-94987630	BJ	skin:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
38	CTCF	chr8:94987827-94987912	GM13977	blood:	n/a	n/a
39	CTCF	chr8:94987500-94987650	GM12873	blood:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
40	CTCF	chr8:94987440-94987590	HMEC	breast:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
41	CTCF	chr8:94987480-94987630	GM12864	blood:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
42	CTCF	chr8:94987360-94987510	A549	lung:	n/a	n/a
43	CTCF	chr8:94987520-94987670	Caco-2	colon:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
44	CTCF	chr8:94987357-94987745	K562	blood:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
45	CTCF	chr8:94987500-94987650	HFF-Myc	foreskin:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
46	CTCF	chr8:94987480-94987630	HUVEC	blood vessel:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
47	CTCF	chr8:94987422-94987721	K562	blood:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
48	CTCF	chr8:94987480-94987630	HMEC	breast:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
49	CTCF	chr8:94987460-94987610	NHLF	lung:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577
50	CTCF	chr8:94987460-94987610	BE2_C	brain:	n/a	chr8:94987554-94987575 chr8:94987561-94987574 chr8:94987560-94987576 chr8:94987559-94987577

No.	Distal block	Cell Line	Cell type
1	chr8:94928011..94930237-chr8:94986282..94987918,2	MCF-7	breast:
2	chr8:94706032..94706941-chr8:94987049..94988013,6	MCF-7	breast:
3	chr8:94834240..94835236-chr8:94986891..94987651,6	K562	blood:
4	chr8:94706225..94706994-chr8:94987102..94988018,5	K562	blood:
5	chr8:94928511..94930316-chr8:94990324..94992311,2	MCF-7	breast:
6	chr8:94705840..94710154-chr8:94987193..94989140,3	MCF-7	breast:
7	chr8:94987851..94989359-chr8:94989772..94991888,2	MCF-7	breast:
8	chr8:94928275..94930362-chr8:94987422..94989757,2	MCF-7	breast:
9	chr8:94577380..94578327-chr8:94987091..94988044,4	MCF-7	breast:
10	chr8:94987851..94989359-chr8:94989772..94991888,2	MCF-7	breast:
11	chr8:94967615..94969465-chr8:94986791..94988525,2	MCF-7	breast:
12	chr8:94834234..94835361-chr8:94986945..94988056,10	MCF-7	breast:
13	chr8:94834485..94835366-chr8:94987131..94988250,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000263855	TF binding region
ENSG00000164951	chromatin interactions
ENSG00000264448	chromatin interactions

Extended variants
information (count: 252 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:252 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7817292	chr8:94985722-94985723	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536061762	chr8:94985733-94985734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570244086	chr8:94985780-94985781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10956891	chr8:94985781-94985782	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs575387667	chr8:94985788-94985789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537797901	chr8:94985861-94985862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557985487	chr8:94985910-94985911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568025670	chr8:94985922-94985923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577969986	chr8:94985976-94985977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183400785	chr8:94985994-94985995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7840040	chr8:94986041-94986042	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs556985032	chr8:94986062-94986063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs58914362	chr8:94986063-94986064	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs11990284	chr8:94986092-94986093	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs192844927	chr8:94986100-94986101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs66645171	chr8:94986131-94986132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535223274	chr8:94986136-94986137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565531058	chr8:94986146-94986147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563241131	chr8:94986214-94986215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546160332	chr8:94986219-94986220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566108809	chr8:94986223-94986224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143246796	chr8:94986241-94986242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548665259	chr8:94986279-94986280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553269095	chr8:94986369-94986370	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs76813763	chr8:94986391-94986392	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs143786452	chr8:94986400-94986401	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs368870011	chr8:94986402-94986403	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs201398573	chr8:94986433-94986434	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs56731732	chr8:94986454-94986455	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs374687107	chr8:94986455-94986456	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs11997800	chr8:94986456-94986457	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs116406850	chr8:94986493-94986494	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs558126982	chr8:94986538-94986539	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs577844644	chr8:94986549-94986550	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs11997831	chr8:94986567-94986568	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs554240210	chr8:94986577-94986578	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs10464832	chr8:94986667-94986668	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs543189699	chr8:94986686-94986687	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs562952623	chr8:94986690-94986691	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs369450862	chr8:94986721-94986722	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs371887919	chr8:94986783-94986784	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs73692985	chr8:94986788-94986789	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs368320689	chr8:94986792-94986793	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs528006051	chr8:94986814-94986815	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs541317126	chr8:94986818-94986819	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs372934447	chr8:94986827-94986828	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs141936065	chr8:94986909-94986910	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs185326564	chr8:94986952-94986953	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs548679434	chr8:94986987-94986988	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs568901582	chr8:94987003-94987004	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
Acute lymphoblastic leukemia	18458336	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

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:94984600-94986400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr8:94984600-94987200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr8:94986400-94986600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr8:94986600-94987000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr8:94986600-94987400	Enhancers	Fetal Intestine Small	intestine
6	chr8:94986800-94987400	Enhancers	Fetal Intestine Large	intestine
7	chr8:94987000-94987800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
8	chr8:94987200-94987600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
9	chr8:94987400-94987800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr8:94987400-94989600	Weak transcription	Fetal Intestine Small	intestine
11	chr8:94987400-94991200	Weak transcription	Fetal Intestine Large	intestine
12	chr8:94987800-94990400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr8:94989600-94994400	Enhancers	Fetal Intestine Small	intestine
14	chr8:94989800-94990800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr8:94990600-94990800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr8:94990800-94992000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr8:94991000-94991400	Enhancers	HMEC	breast
18	chr8:94991200-94991800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr8:94991200-94992600	Enhancers	Gastric	stomach
20	chr8:94991200-94993000	Enhancers	Pancreas	Pancrea
21	chr8:94991200-94993200	Enhancers	Stomach Mucosa	stomach
22	chr8:94991200-94993600	Enhancers	Ovary	ovary
23	chr8:94991200-94994400	Enhancers	Fetal Intestine Large	intestine
24	chr8:94991400-94992400	Enhancers	Placenta	Placenta
25	chr8:94991400-94993400	Enhancers	Fetal Lung	lung
26	chr8:94991400-94993400	Weak transcription	HMEC	breast
27	chr8:94991600-94993200	Enhancers	Duodenum Smooth Muscle	Duodenum
28	chr8:94991800-94992000	Enhancers	Duodenum Mucosa	Duodenum
29	chr8:94991800-94992200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr8:94991800-94992400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr8:94991800-94992400	Enhancers	Colonic Mucosa	Colon
32	chr8:94991800-94992400	Enhancers	Esophagus	oesophagus
33	chr8:94991800-94992400	Enhancers	Left Ventricle	heart
34	chr8:94991800-94992400	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr8:94991800-94992400	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr8:94991800-94992600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr8:94991800-94992600	Enhancers	Lung	lung
38	chr8:94991800-94992600	Enhancers	Right Atrium	heart
39	chr8:94991800-94992800	Enhancers	Fetal Stomach	stomach
40	chr8:94991800-94993000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr8:94991800-94993000	Enhancers	Liver	Liver
42	chr8:94991800-94993000	Enhancers	Brain Hippocampus Middle	brain
43	chr8:94991800-94993000	Enhancers	Brain Substantia Nigra	brain
44	chr8:94991800-94993200	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr8:94991800-94993200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr8:94991800-94993200	Enhancers	Colon Smooth Muscle	Colon
47	chr8:94991800-94993400	Enhancers	Stomach Smooth Muscle	stomach
48	chr8:94991800-94993600	Enhancers	Right Ventricle	heart
49	chr8:94992000-94992200	Enhancers	Brain Germinal Matrix	brain
50	chr8:94992000-94992400	Enhancers	Aorta	Aorta

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