Variant report

Variant	nsv611690
Chromosome Location	chr8:87188869-87193911
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	E2F4	chr8:87188803-87188979	MCF10A-Er-Src	breast:	n/a	n/a
2	EP300	chr8:87188997-87189386	SK-N-SH_RA	brain:	n/a	chr8:87189048-87189061 chr8:87189194-87189203
3	EP300	chr8:87189025-87189384	SK-N-SH_RA	brain:	n/a	chr8:87189048-87189061 chr8:87189194-87189203
4	EP300	chr8:87188804-87189398	SK-N-SH	brain:	n/a	chr8:87189048-87189061 chr8:87189194-87189203
5	EP300	chr8:87189054-87189336	Hela-S3	cervix:	n/a	chr8:87189194-87189203
6	FOS	chr8:87188835-87189335	MCF10A-Er-Src	breast:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189192-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
7	FOS	chr8:87188684-87189378	MCF10A-Er-Src	breast:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189192-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
8	FOS	chr8:87188908-87189343	MCF10A-Er-Src	breast:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189192-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
9	FOS	chr8:87188768-87189386	MCF10A-Er-Src	breast:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189192-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
10	FOS	chr8:87188778-87189577	HUVEC	blood vessel:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189192-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
11	FOSL1	chr8:87188598-87189574	HCT-116	colon:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
12	FOSL1	chr8:87188728-87189476	HCT-116	colon:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
13	FOSL2	chr8:87188664-87189453	A549	lung:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
14	FOSL2	chr8:87188926-87189439	MCF-7	breast:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
15	FOSL2	chr8:87188740-87189499	SK-N-SH	brain:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
16	FOSL2	chr8:87188877-87189475	MCF-7	breast:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
17	FOSL2	chr8:87188913-87189377	SK-N-SH	brain:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
18	FOSL2	chr8:87189033-87189353	A549	lung:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
19	GATA3	chr8:87188822-87189441	SK-N-SH	brain:	n/a	n/a
20	GATA3	chr8:87192164-87193061	MCF-7	breast:	n/a	n/a
21	GATA3	chr8:87187934-87189005	MCF-7	breast:	n/a	n/a
22	GATA3	chr8:87192417-87193001	MCF-7	breast:	n/a	n/a
23	GATA3	chr8:87187938-87189502	SK-N-SH	brain:	n/a	n/a
24	JUND	chr8:87188826-87189503	SK-N-SH	brain:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
25	JUND	chr8:87188771-87189548	HCT-116	colon:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
26	JUND	chr8:87188732-87189501	SK-N-SH	brain:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
27	JUND	chr8:87188865-87189477	SK-N-SH	brain:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
28	JUND	chr8:87188630-87189489	HCT-116	colon:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
29	MAFK	chr8:87189156-87189283	K562	blood:	n/a	chr8:87189194-87189204
30	MAFK	chr8:87189011-87189308	Hela-S3	cervix:	n/a	chr8:87189194-87189204
31	MYC	chr8:87189107-87189307	MCF10A-Er-Src	breast:	n/a	chr8:87189194-87189203
32	NFIC	chr8:87188821-87189518	SK-N-SH	brain:	n/a	n/a
33	NFIC	chr8:87188863-87189447	ECC-1	luminal epithelium:	n/a	n/a
34	PBX3	chr8:87188915-87189443	SK-N-SH	brain:	n/a	n/a
35	PBX3	chr8:87188839-87189531	SK-N-SH	brain:	n/a	n/a
36	POLR2A	chr8:87192818-87192867	ProgFib	skin:	n/a	n/a
37	POLR2A	chr8:87189013-87189381	SK-N-SH	brain:	n/a	n/a
38	POLR2A	chr8:87188807-87189439	U87	brain:	n/a	n/a
39	RAD21	chr8:87189046-87189344	SK-N-SH_RA	brain:	n/a	n/a
40	RCOR1	chr8:87189057-87189297	Hela-S3	cervix:	n/a	n/a
41	SIN3AK20	chr8:87188025-87189412	MCF-7	breast:	n/a	n/a
42	SMC3	chr8:87189027-87189305	Hela-S3	cervix:	n/a	n/a
43	SP1	chr8:87188690-87189556	HCT-116	colon:	n/a	n/a
44	STAT3	chr8:87188766-87189096	MCF10A-Er-Src	breast:	n/a	chr8:87189013-87189024
45	STAT3	chr8:87192304-87192394	MCF10A-Er-Src	breast:	n/a	n/a
46	TCF12	chr8:87188160-87189499	SK-N-SH	brain:	n/a	n/a
47	TCF12	chr8:87187945-87189484	SK-N-SH	brain:	n/a	n/a
48	TCF12	chr8:87188596-87189475	A549	lung:	n/a	n/a
49	TEAD4	chr8:87188877-87189526	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:87193443..87195770-chr8:87354919..87356635,3	MCF-7	breast:
2	chr8:87192734..87196437-chr8:87354857..87357737,4	MCF-7	breast:
3	chr8:87187097..87192513-chr8:87353340..87357451,6	MCF-7	breast:
4	chr8:87189537..87192109-chr8:87199086..87201093,2	MCF-7	breast:
5	chr8:87188610..87190453-chr8:87196607..87198359,2	MCF-7	breast:
6	chr8:87190469..87192191-chr8:87210663..87212770,3	MCF-7	breast:
7	chr8:87187644..87190858-chr8:87193352..87196070,3	MCF-7	breast:
8	chr8:87187644..87190858-chr8:87193352..87196070,3	MCF-7	breast:
9	chr8:87187218..87190589-chr8:87353304..87356196,4	MCF-7	breast:
10	chr8:87193009..87195641-chr8:87198363..87201280,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V0D2-1	chr8:87192647-87192848	ENSG00000253699.1

Variant related genes	Relation type
ENSG00000253699	TF binding region
ENSG00000123124	chromatin interactions
ENSG00000254231	chromatin interactions

Extended variants
information (count: 174 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:174 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9642877	chr8:87188869-87188870	Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535718058	chr8:87188914-87188915	Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs570201424	chr8:87188976-87188977	Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs75683057	chr8:87188983-87188984	Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs188880395	chr8:87189034-87189035	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs192922881	chr8:87189062-87189063	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs141140190	chr8:87189135-87189136	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs146193453	chr8:87189159-87189160	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs543486243	chr8:87189175-87189176	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs563671491	chr8:87189183-87189184	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs375440763	chr8:87189255-87189256	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs139112776	chr8:87189269-87189270	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs559592604	chr8:87189327-87189328	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs528343719	chr8:87189347-87189348	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs551546340	chr8:87189355-87189356	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs143875476	chr8:87189373-87189374	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs146394621	chr8:87189518-87189519	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs370999456	chr8:87189532-87189533	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs139337765	chr8:87189547-87189548	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs16894336	chr8:87189585-87189586	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs535752454	chr8:87189616-87189617	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs565902551	chr8:87189620-87189621	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs566029012	chr8:87189621-87189622	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs534927397	chr8:87189630-87189631	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs78564975	chr8:87189635-87189636	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs150046626	chr8:87189640-87189641	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs543864935	chr8:87189735-87189736	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs79402645	chr8:87189774-87189775	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs571282718	chr8:87189833-87189834	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs183538654	chr8:87189896-87189897	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs533720038	chr8:87189900-87189901	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs111385789	chr8:87189921-87189922	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs114265279	chr8:87189949-87189950	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs114768548	chr8:87190008-87190009	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs371592499	chr8:87190015-87190016	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs67149475	chr8:87190031-87190032	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs563361090	chr8:87190035-87190036	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs550607655	chr8:87190046-87190047	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs575494143	chr8:87190050-87190051	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs149172065	chr8:87190054-87190055	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs529687541	chr8:87190112-87190113	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs577150008	chr8:87190118-87190119	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs543973385	chr8:87190151-87190152	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs546178621	chr8:87190178-87190179	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs114280651	chr8:87190189-87190190	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs77210239	chr8:87190236-87190237	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs535304362	chr8:87190247-87190248	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs558083728	chr8:87190293-87190294	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs565375341	chr8:87190300-87190301	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs68107928	chr8:87190311-87190312	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	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
Autism	22495311	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
Acute lymphoblastic leukemia	22237106	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	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
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
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:87186200-87189200	Enhancers	HepG2	liver
2	chr8:87187000-87189800	Enhancers	Hela-S3	cervix
3	chr8:87187600-87189000	Enhancers	Fetal Lung	lung
4	chr8:87187600-87189800	Enhancers	Placenta Amnion	Placenta Amnion
5	chr8:87187800-87189400	Enhancers	Osteobl	bone
6	chr8:87187800-87190000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr8:87188000-87189000	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr8:87188000-87189200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr8:87188000-87189200	Flanking Active TSS	A549	lung
10	chr8:87188000-87189200	Flanking Active TSS	NH-A	brain
11	chr8:87188000-87189400	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr8:87188000-87189400	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chr8:87188000-87189400	Flanking Active TSS	HUVEC	blood vessel
14	chr8:87188200-87189000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr8:87188200-87189000	Enhancers	Fetal Heart	heart
16	chr8:87188200-87189200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
17	chr8:87188200-87189200	Flanking Active TSS	NHEK	skin
18	chr8:87188200-87189400	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr8:87188200-87189400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr8:87188200-87189400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr8:87188200-87189400	Enhancers	Brain Cingulate Gyrus	brain
22	chr8:87188200-87189400	Flanking Active TSS	HMEC	breast
23	chr8:87188200-87189400	Enhancers	NHDF-Ad	bronchial
24	chr8:87188200-87190000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr8:87188400-87189000	Enhancers	Rectal Smooth Muscle	rectum
26	chr8:87188400-87189200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr8:87188400-87189400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr8:87188400-87189400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr8:87188400-87189400	Enhancers	Brain Anterior Caudate	brain
30	chr8:87188400-87189800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr8:87188600-87189000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr8:87188600-87189400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr8:87188800-87189000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr8:87188800-87189000	Enhancers	HSMM	muscle
35	chr8:87188800-87189000	Flanking Active TSS	HSMMtube	muscle
36	chr8:87188800-87189200	Enhancers	Brain Substantia Nigra	brain
37	chr8:87188800-87189400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr8:87189000-87189200	Flanking Active TSS	HSMM	muscle
39	chr8:87189000-87189400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr8:87189000-87189400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr8:87189000-87189400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr8:87189000-87189400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr8:87189000-87189800	Enhancers	HSMMtube	muscle
44	chr8:87189200-87189600	Weak transcription	Fetal Lung	lung
45	chr8:87189200-87189800	Enhancers	Muscle Satellite Cultured Cells	--
46	chr8:87189200-87189800	Enhancers	HSMM	muscle
47	chr8:87189200-87189800	Enhancers	NH-A	brain
48	chr8:87189200-87190200	Enhancers	A549	lung
49	chr8:87189200-87190400	Enhancers	NHEK	skin
50	chr8:87189400-87189600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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