Variant report

Variant	nsv1034700
Chromosome Location	chr8:86843256-86900652
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:604)
CpG islands
(count:0)
Chromatin interactive
region (count:76)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:604 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:86854067-86854193	K562	blood:	n/a	n/a
2	ARID3A	chr8:86860674-86860711	K562	blood:	n/a	n/a
3	ARID3A	chr8:86868281-86868466	K562	blood:	n/a	n/a
4	ARID3A	chr8:86860947-86861211	K562	blood:	n/a	n/a
5	ARID3A	chr8:86848202-86848466	K562	blood:	n/a	n/a
6	ARID3A	chr8:86873919-86874476	K562	blood:	n/a	n/a
7	ARID3A	chr8:86877891-86877975	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:86855400-86856788	K562	blood:	n/a	chr8:86856408-86856424
9	ARID3A	chr8:86860057-86860260	K562	blood:	n/a	n/a
10	ARID3A	chr8:86851632-86852291	K562	blood:	n/a	n/a
11	ARID3A	chr8:86878872-86879538	K562	blood:	n/a	n/a
12	ATF1	chr8:86851680-86851940	K562	blood:	n/a	n/a
13	ATF1	chr8:86858572-86858850	K562	blood:	n/a	n/a
14	ATF3	chr8:86848176-86848532	K562	blood:	n/a	n/a
15	ATF3	chr8:86853960-86854338	K562	blood:	n/a	n/a
16	BACH1	chr8:86854704-86854857	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr8:86848360-86848557	K562	blood:	n/a	n/a
18	BACH1	chr8:86855556-86855909	K562	blood:	n/a	n/a
19	BACH1	chr8:86873787-86874392	K562	blood:	n/a	n/a
20	BACH1	chr8:86873756-86874253	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr8:86878970-86879079	K562	blood:	n/a	n/a
22	BHLHE40	chr8:86864850-86864971	K562	blood:	n/a	n/a
23	BHLHE40	chr8:86851452-86852081	K562	blood:	n/a	n/a
24	BHLHE40	chr8:86860851-86861210	K562	blood:	n/a	n/a
25	BHLHE40	chr8:86848213-86848489	K562	blood:	n/a	n/a
26	BHLHE40	chr8:86878900-86879572	K562	blood:	n/a	n/a
27	CBX3	chr8:86878808-86879237	K562	blood:	n/a	n/a
28	CBX3	chr8:86848116-86848555	K562	blood:	n/a	n/a
29	CBX3	chr8:86882637-86883016	K562	blood:	n/a	n/a
30	CBX3	chr8:86855246-86855994	K562	blood:	n/a	n/a
31	CCNT2	chr8:86878585-86879466	K562	blood:	n/a	chr8:86879008-86879028
32	CCNT2	chr8:86855767-86856007	K562	blood:	n/a	n/a
33	CCNT2	chr8:86898116-86898307	K562	blood:	n/a	n/a
34	CCNT2	chr8:86851412-86851908	K562	blood:	n/a	n/a
35	CEBPB	chr8:86874304-86874672	HepG2	liver:	n/a	chr8:86874482-86874493
36	CEBPB	chr8:86874335-86874656	H1-hESC	embryonic stem cell:	n/a	chr8:86874482-86874493
37	CEBPB	chr8:86848151-86848550	ECC-1	luminal epithelium:	n/a	chr8:86848372-86848383
38	CEBPB	chr8:86852999-86853917	MCF-7	breast:	n/a	chr8:86853134-86853151
39	CEBPB	chr8:86874267-86874692	ECC-1	luminal epithelium:	n/a	chr8:86874482-86874493
40	CEBPB	chr8:86855387-86855903	K562	blood:	n/a	n/a
41	CEBPB	chr8:86847845-86848785	K562	blood:	n/a	chr8:86848372-86848383
42	CEBPB	chr8:86853219-86853518	K562	blood:	n/a	n/a
43	CEBPB	chr8:86848166-86848569	HepG2	liver:	n/a	chr8:86848372-86848383
44	CEBPB	chr8:86848192-86848660	H1-hESC	embryonic stem cell:	n/a	chr8:86848372-86848383
45	CEBPB	chr8:86874027-86874656	Hela-S3	cervix:	n/a	chr8:86874482-86874493
46	CEBPB	chr8:86874268-86874695	ECC-1	luminal epithelium:	n/a	chr8:86874482-86874493
47	CEBPB	chr8:86858744-86859178	K562	blood:	n/a	chr8:86858989-86859000
48	CEBPB	chr8:86848109-86848565	ECC-1	luminal epithelium:	n/a	chr8:86848372-86848383
49	CEBPB	chr8:86848095-86848658	HCT-116	colon:	n/a	chr8:86848372-86848383
50	CEBPB	chr8:86847697-86849448	Hela-S3	cervix:	n/a	chr8:86848372-86848383

No data

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:86864135..86865739-chr8:86867994..86869726,2	K562	blood:
2	chr8:86865679..86869782-chr8:86870364..86872343,3	MCF-7	breast:
3	chr8:86852831..86853539-chr8:86919503..86920015,2	MCF-7	breast:
4	chr8:86864951..86867156-chr8:86950288..86952196,2	K562	blood:
5	chr8:86866655..86868927-chr8:86870590..86874049,3	K562	blood:
6	chr8:86866810..86870482-chr8:86870568..86874255,4	K562	blood:
7	chr8:86890525..86892195-chr8:86896949..86899068,2	MCF-7	breast:
8	chr8:86863160..86866224-chr8:86868226..86872946,5	K562	blood:
9	chr8:86854583..86856864-chr8:86887493..86890271,2	MCF-7	breast:
10	chr8:86865438..86867152-chr8:86874296..86876870,2	MCF-7	breast:
11	chr8:86853963..86856746-chr8:86949985..86952408,2	K562	blood:
12	chr8:86854974..86856986-chr8:86861959..86864314,2	MCF-7	breast:
13	chr8:86887935..86890742-chr8:86895465..86898083,2	MCF-7	breast:
14	chr8:86849344..86852342-chr8:86863151..86865379,2	K562	blood:
15	chr8:86853468..86855962-chr8:86866121..86867816,2	MCF-7	breast:
16	chr3:61613244..61613971-chr8:86852933..86853873,2	MCF-7	breast:
17	chr8:86863160..86866224-chr8:86868226..86872946,5	K562	blood:
18	chr8:86372229..86378702-chr8:86846475..86858080,32	MCF-7	breast:
19	chr8:86887935..86890742-chr8:86895465..86898083,2	MCF-7	breast:
20	chr8:86865438..86867152-chr8:86874296..86876870,2	MCF-7	breast:
21	chr8:86852831..86853452-chr8:86919492..86920015,2	MCF-7	breast:
22	chr8:86866655..86868927-chr8:86870590..86874049,3	K562	blood:
23	chr8:86865679..86869782-chr8:86870364..86872343,3	MCF-7	breast:
24	chr8:86364996..86367147-chr8:86853567..86855147,2	MCF-7	breast:
25	chr8:86896571..86899286-chr8:86899613..86901432,2	K562	blood:
26	chr8:86890568..86892933-chr8:86896253..86899080,2	K562	blood:
27	chr8:86855854..86858675-chr8:86858692..86862985,4	K562	blood:
28	chr8:86867877..86870175-chr8:86957602..86960658,3	K562	blood:
29	chr8:86873909..86875817-chr8:86877327..86879783,3	K562	blood:
30	chr8:86887769..86891314-chr8:86899255..86902657,3	MCF-7	breast:
31	chr8:86853239..86855144-chr8:86935082..86937255,2	MCF-7	breast:
32	chr8:86864135..86865739-chr8:86867994..86869726,2	K562	blood:
33	chr8:86375109..86376361-chr8:86852746..86853757,4	MCF-7	breast:
34	chr8:86842328..86846143-chr8:86846375..86849662,4	K562	blood:
35	chr8:86849418..86851109-chr8:86874092..86876828,2	MCF-7	breast:
36	chr8:86855854..86858675-chr8:86858692..86862985,4	K562	blood:
37	chr8:86855992..86858469-chr8:86859660..86861283,2	MCF-7	breast:
38	chr8:86855992..86858469-chr8:86859660..86861283,2	MCF-7	breast:
39	chr8:86876992..86879169-chr8:86912945..86915050,2	K562	blood:
40	chr8:86853239..86855562-chr8:86941096..86942635,2	MCF-7	breast:
41	chr8:86843222..86846042-chr8:86847745..86849520,2	K562	blood:
42	chr8:86847849..86857260-chr8:86866079..86880479,25	MCF-7	breast:
43	chr8:86849418..86851109-chr8:86874092..86876828,2	MCF-7	breast:
44	chr8:86868209..86870416-chr8:86917445..86919044,2	K562	blood:
45	chr8:86854974..86856986-chr8:86861959..86864314,2	MCF-7	breast:
46	chr8:86375074..86376045-chr8:86894229..86895117,2	MCF-7	breast:
47	chr8:86873909..86875817-chr8:86877327..86879783,3	K562	blood:
48	chr8:86376110..86377714-chr8:86896432..86898770,2	MCF-7	breast:
49	chr16:75285561..75287264-chr8:86851129..86852972,2	MCF-7	breast:
50	chr8:86854583..86856864-chr8:86887493..86890271,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V0D2-2	chr8:86851934-86852014	NONHSAT127540
2	lnc-REXO1L2P-2	chr8:86866739-86866829	XLOC_007141
3	lnc-ATP6V0D2-2	chr8:86851934-86852014	ENSG00000253154
4	lnc-ATP6V0D2-2	chr8:86898164-86898223	NONHSAT127540
5	lnc-ATP6V0D2-2	chr8:86898164-86898223	ENSG00000253154
6	lnc-REXO1L2P-2	chr8:86864119-86865001	XLOC_007141

No data

Variant related genes	Relation type
ENSG00000253154	TF binding region
REXO1L2P	TF binding region
ENSG00000254231	chromatin interactions
ENSG00000253549	chromatin interactions
ENSG00000253154	chromatin interactions
ENSG00000123124	chromatin interactions
ENSG00000104267	chromatin interactions
ENSG00000050820	chromatin interactions

Extended variants
information (count: 1980 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:1980 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564043515	chr8:86843262-86843263	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs532944641	chr8:86843280-86843281	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs148300881	chr8:86843297-86843298	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs549938795	chr8:86843301-86843302	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs199770745	chr8:86843312-86843313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569797321	chr8:86843334-86843335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535515585	chr8:86843388-86843389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547909824	chr8:86843418-86843419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549135960	chr8:86843493-86843494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34620230	chr8:86843499-86843500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs80085992	chr8:86843611-86843612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35102317	chr8:86843615-86843616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs146285612	chr8:86843616-86843617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs77460195	chr8:86843617-86843618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577601047	chr8:86843622-86843623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542144892	chr8:86843654-86843655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563823878	chr8:86843658-86843659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539788378	chr8:86843678-86843679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556693013	chr8:86843689-86843690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531175274	chr8:86843736-86843737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562935427	chr8:86843768-86843769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530471417	chr8:86843769-86843770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576593092	chr8:86843770-86843771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542273809	chr8:86843826-86843827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192123651	chr8:86843841-86843842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs118156374	chr8:86843865-86843866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182361056	chr8:86843888-86843889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186797521	chr8:86843965-86843966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139292203	chr8:86844013-86844014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549838060	chr8:86844016-86844017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563484493	chr8:86844023-86844024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs376910362	chr8:86844047-86844048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73265467	chr8:86844107-86844108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142595019	chr8:86844109-86844110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190319694	chr8:86844123-86844124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546681241	chr8:86844143-86844144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs115159489	chr8:86844163-86844164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528234764	chr8:86844182-86844183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs146006126	chr8:86844211-86844212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568093132	chr8:86844304-86844305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571180784	chr8:86844340-86844341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182612780	chr8:86844346-86844347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs540110406	chr8:86844406-86844407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs35340721	chr8:86844440-86844441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556594319	chr8:86844462-86844463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139497631	chr8:86844485-86844486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186888636	chr8:86844615-86844616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190054213	chr8:86844626-86844627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182300540	chr8:86844632-86844633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570685944	chr8:86844634-86844635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

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
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21030649	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

Chromatin state (count:882 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86841000-86844600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:86841000-86845000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:86841200-86844200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr8:86841200-86845000	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr8:86841600-86844200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr8:86841800-86843400	Enhancers	Brain Substantia Nigra	brain
7	chr8:86841800-86843600	Enhancers	Brain Anterior Caudate	brain
8	chr8:86842200-86843400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr8:86842200-86843400	Enhancers	Brain Cingulate Gyrus	brain
10	chr8:86842200-86843600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:86842200-86843600	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr8:86842200-86843800	Enhancers	Fetal Lung	lung
13	chr8:86842400-86844000	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr8:86842800-86843400	Enhancers	NHEK	skin
15	chr8:86842800-86843600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr8:86842800-86843600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr8:86842800-86843600	Enhancers	HMEC	breast
18	chr8:86842800-86843800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr8:86842800-86843800	Enhancers	Placenta Amnion	Placenta Amnion
20	chr8:86842800-86845200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:86843000-86843800	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr8:86843000-86844000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr8:86843000-86844800	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr8:86843000-86845800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr8:86843000-86846000	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr8:86843000-86846800	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr8:86843000-86847200	Weak transcription	Brain Hippocampus Middle	brain
28	chr8:86843000-86848600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr8:86843000-86848800	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr8:86843200-86843800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr8:86843200-86844800	Weak transcription	K562	blood
32	chr8:86843200-86848400	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr8:86843400-86844800	Weak transcription	Brain Substantia Nigra	brain
34	chr8:86843400-86845600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr8:86843400-86847000	Weak transcription	NHEK	skin
36	chr8:86843600-86845600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr8:86843600-86846800	Weak transcription	HMEC	breast
38	chr8:86843600-86847000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr8:86843600-86847600	Weak transcription	Brain Anterior Caudate	brain
40	chr8:86843600-86847800	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr8:86843600-86849000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr8:86843800-86844000	Enhancers	Placenta	Placenta
43	chr8:86843800-86845800	Weak transcription	Fetal Lung	lung
44	chr8:86843800-86846800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr8:86843800-86846800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr8:86843800-86846800	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr8:86843800-86847000	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr8:86844000-86847800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr8:86844200-86846800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr8:86844200-86849200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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