Variant report

Variant	esv3366503
Chromosome Location	chr6:87849282-87862940
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:378)
CpG islands
(count:305)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:87861450-87862698	GM12878	blood:	n/a	n/a
2	BACH1	chr6:87861374-87862164	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr6:87856067-87856352	GM12878	blood:	n/a	n/a
4	BCLAF1	chr6:87861326-87862508	GM12878	blood:	n/a	chr6:87861592-87861601 chr6:87861960-87861968 chr6:87862035-87862048 chr6:87861583-87861596
5	BCLAF1	chr6:87861428-87862334	GM12878	blood:	n/a	chr6:87861592-87861601 chr6:87861960-87861968 chr6:87862035-87862048 chr6:87861583-87861596
6	BHLHE40	chr6:87861139-87862710	GM12878	blood:	n/a	chr6:87861585-87861601
7	CEBPB	chr6:87850052-87850255	HepG2	liver:	n/a	n/a
8	CEBPD	chr6:87849032-87849420	K562	blood:	n/a	n/a
9	CHD1	chr6:87861185-87862694	GM12878	blood:	n/a	n/a
10	CHD1	chr6:87861895-87862175	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr6:87861214-87862623	GM12878	blood:	n/a	n/a
12	CHD2	chr6:87861590-87862324	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr6:87861496-87862335	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTBP2	chr6:87861434-87862487	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr6:87861520-87861670	AG09319	gingival:	n/a	chr6:87861635-87861644 chr6:87861631-87861644
16	CTCF	chr6:87861760-87861910	BJ	skin:	n/a	n/a
17	CTCF	chr6:87852606-87852663	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr6:87861600-87861750	GM12865	blood:	n/a	chr6:87861635-87861644 chr6:87861631-87861644
19	CTCF	chr6:87861620-87861770	GM12871	blood:	n/a	chr6:87861635-87861644 chr6:87861631-87861644
20	CTCF	chr6:87861500-87861650	SK-N-SH_RA	brain:	n/a	chr6:87861635-87861644 chr6:87861631-87861644
21	CTCF	chr6:87861540-87861690	HUVEC	blood vessel:	n/a	chr6:87861635-87861644 chr6:87861631-87861644
22	CTCF	chr6:87861897-87862047	GM12891	blood:	n/a	n/a
23	CTCF	chr6:87861760-87861910	GM12864	blood:	n/a	n/a
24	CTCF	chr6:87861500-87861650	GM12871	blood:	n/a	chr6:87861635-87861644 chr6:87861631-87861644
25	CTCF	chr6:87861560-87861710	AG04449	skin:	n/a	chr6:87861635-87861644 chr6:87861631-87861644
26	CTCF	chr6:87848845-87849392	A549	lung:	n/a	n/a
27	CTCF	chr6:87859300-87859450	Caco-2	colon:	n/a	n/a
28	CTCF	chr6:87861840-87861990	GM12878	blood:	n/a	n/a
29	CTCF	chr6:87861960-87862110	GM12871	blood:	n/a	n/a
30	CTCF	chr6:87848931-87849317	A549	lung:	n/a	n/a
31	CTCF	chr6:87848887-87849488	MCF-7	breast:	n/a	n/a
32	CTCF	chr6:87861460-87861610	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr6:87849031-87849282	ECC-1	luminal epithelium:	n/a	n/a
34	CTCF	chr6:87861840-87861990	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr6:87849009-87849301	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr6:87861780-87861930	GM12874	blood:	n/a	n/a
37	CTCF	chr6:87861540-87861690	HMEC	breast:	n/a	chr6:87861635-87861644 chr6:87861631-87861644
38	CTCF	chr6:87848895-87849348	HepG2	liver:	n/a	n/a
39	CTCF	chr6:87861871-87862005	GM19238	blood:	n/a	n/a
40	CTCF	chr6:87861800-87861950	AG04449	skin:	n/a	n/a
41	CTCF	chr6:87848997-87849295	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr6:87861800-87861950	GM12865	blood:	n/a	n/a
43	CTCF	chr6:87861900-87862050	GM12865	blood:	n/a	n/a
44	CTCF	chr6:87861640-87861790	GM12870	blood:	n/a	n/a
45	CTCF	chr6:87861640-87861699	GM10266	blood:	n/a	n/a
46	CTCF	chr6:87861840-87861990	Caco-2	colon:	n/a	n/a
47	CTCF	chr6:87848869-87849426	HCT-116	colon:	n/a	n/a
48	CTCF	chr6:87861860-87862024	GM12892	blood:	n/a	n/a
49	CTCF	chr6:87861679-87861697	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:87861820-87861970	SK-N-SH_RA	brain:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:87862264-87862314	HCF	heart:	n/a
2	chr6:87862158-87862208	K562	blood:	n/a
3	chr6:87861586-87861636	GM06990	blood:	n/a
4	chr6:87859404-87859454	ProgFib	skin:	n/a
5	chr6:87862264-87862314	NH-A	brain:	n/a
6	chr6:87859404-87859454	NHBE	bronchial:	n/a
7	chr6:87862264-87862314	Jurkat	blood:	n/a
8	chr6:87861261-87861311	H1-hESC	embryonic stem cell:	embryo
9	chr6:87861586-87861636	NH-A	brain:	n/a
10	chr6:87862264-87862314	AG09309	skin:	n/a
11	chr6:87861261-87861311	HEEpiC	esophagus:	n/a
12	chr6:87861586-87861636	PANC-1	pancreas:	n/a
13	chr6:87859404-87859454	AG04449	skin:	fetal
14	chr6:87862158-87862208	GM12878	blood:	n/a
15	chr6:87862158-87862208	ovcar-3	ovarian:	n/a
16	chr6:87862158-87862208	NH-A	brain:	n/a
17	chr6:87862158-87862208	PFSK-1	brain:	n/a
18	chr6:87861261-87861311	MCF10A-Er-Src	breast:	n/a
19	chr6:87859404-87859454	HUVEC	blood vessel:	n/a
20	chr6:87862264-87862314	CMK	blood:	n/a
21	chr6:87862264-87862314	K562	blood:	n/a
22	chr6:87861261-87861311	GM12891	blood:	n/a
23	chr6:87862158-87862208	SK-N-MC	brain:	n/a
24	chr6:87861261-87861311	GM06990	blood:	n/a
25	chr6:87861586-87861636	A549	lung:	n/a
26	chr6:87862264-87862314	HCM	heart:	n/a
27	chr6:87862264-87862314	BE2_C	brain:	n/a
28	chr6:87862158-87862208	HCT-116	colon:	n/a
29	chr6:87861261-87861311	AG09309	skin:	n/a
30	chr6:87862158-87862208	HUVEC	blood vessel:	n/a
31	chr6:87859404-87859454	SKMC	muscle:	n/a
32	chr6:87861261-87861311	SK-N-MC	brain:	n/a
33	chr6:87861586-87861636	RPTEC	kidney:	n/a
34	chr6:87862158-87862208	MCF10A-Er-Src	breast:	n/a
35	chr6:87859404-87859454	PANC-1	pancreas:	n/a
36	chr6:87859404-87859454	Jurkat	blood:	n/a
37	chr6:87861261-87861311	AG04449	skin:	fetal
38	chr6:87862158-87862208	AG10803	skin:	n/a
39	chr6:87861586-87861636	HIPEpiC	eye:	n/a
40	chr6:87859404-87859454	HPAEpiC	pulmonary alveolar:	n/a
41	chr6:87861261-87861311	NB4	blood:	n/a
42	chr6:87861261-87861311	HIPEpiC	eye:	n/a
43	chr6:87861586-87861636	H1-hESC	embryonic stem cell:	embryo
44	chr6:87859404-87859454	U87	brain:	n/a
45	chr6:87862264-87862314	T-47D	breast:	n/a
46	chr6:87861261-87861311	ECC-1	luminal epithelium:	n/a
47	chr6:87861261-87861311	BJ	skin:	n/a
48	chr6:87861586-87861636	PrEC	prostate:	n/a
49	chr6:87861261-87861311	HL-60	blood:	n/a
50	chr6:87861261-87861311	K562	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:87848965..87849598-chr6:87947375..87947982,2	MCF-7	breast:
2	chr6:87856173..87858618-chr6:87861857..87866815,6	MCF-7	breast:
3	chr6:86386962..86389714-chr6:87862273..87864563,2	MCF-7	breast:
4	chr6:87857695..87859614-chr6:87863756..87866185,3	K562	blood:
5	chr6:87862757..87864268-chr6:87915198..87917415,2	MCF-7	breast:
6	chr6:87855485..87860129-chr6:87863534..87866508,4	K562	blood:
7	chr6:87848849..87849529-chr6:87950710..87951578,2	MCF-7	breast:
8	chr6:87848708..87849374-chr6:87947267..87947811,2	MCF-7	breast:
9	chr6:87860967..87863617-chr6:87863794..87865835,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CGA-2	chr6:87860877-87865003	ENSG00000272008.1

No data

Variant related genes	Relation type
ZNF292	TF binding region
ZNF292	CpG island
ENSG00000272008	chromatin interactions
ENSG00000203875	chromatin interactions
ENSG00000188994	chromatin interactions

Extended variants
information (count: 502 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546888749	chr6:87849311-87849312	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs144436634	chr6:87849394-87849395	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185854899	chr6:87849442-87849443	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376626959	chr6:87849453-87849454	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs111812472	chr6:87849460-87849461	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs368375702	chr6:87849471-87849472	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539604927	chr6:87849486-87849487	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558027031	chr6:87849494-87849495	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190228262	chr6:87849498-87849499	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534033741	chr6:87849499-87849500	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs555711882	chr6:87849500-87849501	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142431733	chr6:87849514-87849515	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541881437	chr6:87849536-87849537	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530139529	chr6:87849545-87849546	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575688274	chr6:87849548-87849549	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546373455	chr6:87849558-87849559	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs117488872	chr6:87849566-87849567	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528668740	chr6:87849575-87849576	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs57962992	chr6:87849591-87849592	ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs562066307	chr6:87849592-87849593	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528858739	chr6:87849656-87849657	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs145975582	chr6:87849679-87849680	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs139898755	chr6:87849706-87849707	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs113310527	chr6:87849733-87849734	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551504026	chr6:87849745-87849746	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566630826	chr6:87849758-87849759	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533995107	chr6:87849762-87849763	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs117485079	chr6:87849782-87849783	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573882574	chr6:87849805-87849806	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539208917	chr6:87849808-87849809	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs386703497	chr6:87849845-87849846	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7751029	chr6:87849847-87849848	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs113075231	chr6:87849870-87849871	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545848823	chr6:87849880-87849881	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564254168	chr6:87849881-87849882	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569569385	chr6:87849889-87849890	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs180854542	chr6:87849913-87849914	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145698753	chr6:87849922-87849923	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs13200791	chr6:87849971-87849972	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557005884	chr6:87849993-87849994	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369251986	chr6:87849994-87849995	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555073664	chr6:87850115-87850116	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529600536	chr6:87850129-87850130	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375654661	chr6:87850130-87850131	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141568183	chr6:87850177-87850178	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs62439494	chr6:87850182-87850183	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs554751900	chr6:87850191-87850192	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532952322	chr6:87850226-87850227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs142795289	chr6:87850316-87850317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56942939	chr6:87850321-87850322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
Myelodysplastic syndrome	18508791	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	21364760	CNVD
Developmental delay	19490664	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:440 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:87849200-87849400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
2	chr6:87849200-87849400	Enhancers	Hela-S3	cervix
3	chr6:87849200-87849800	Enhancers	HepG2	liver
4	chr6:87849400-87850200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:87849800-87855600	Weak transcription	HepG2	liver
6	chr6:87855600-87855800	Enhancers	HepG2	liver
7	chr6:87855600-87856600	Active TSS	GM12878-XiMat	blood
8	chr6:87855800-87856400	Active TSS	Brain Hippocampus Middle	brain
9	chr6:87856000-87856400	Active TSS	Brain Cingulate Gyrus	brain
10	chr6:87856400-87860800	Weak transcription	Brain Cingulate Gyrus	brain
11	chr6:87856600-87860800	Weak transcription	GM12878-XiMat	blood
12	chr6:87858200-87858600	Enhancers	HUVEC	blood vessel
13	chr6:87858600-87861200	Weak transcription	HUVEC	blood vessel
14	chr6:87860600-87860800	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr6:87860600-87860800	Enhancers	Brain Anterior Caudate	brain
16	chr6:87860800-87861000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr6:87860800-87861000	Flanking Active TSS	Brain Anterior Caudate	brain
18	chr6:87860800-87861000	Enhancers	Brain Germinal Matrix	brain
19	chr6:87860800-87861000	Enhancers	GM12878-XiMat	blood
20	chr6:87860800-87861200	Enhancers	Brain Cingulate Gyrus	brain
21	chr6:87860800-87861200	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr6:87860800-87861200	Enhancers	Brain Substantia Nigra	brain
23	chr6:87860800-87862400	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr6:87860800-87862800	Active TSS	Pancreatic Islets	Pancreatic Islet
25	chr6:87861000-87861200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr6:87861000-87861200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
27	chr6:87861000-87861200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
28	chr6:87861000-87861200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:87861000-87861200	Enhancers	Primary B cells from peripheral blood	blood
30	chr6:87861000-87861200	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr6:87861000-87861200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr6:87861000-87861200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr6:87861000-87861200	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr6:87861000-87861200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr6:87861000-87861200	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr6:87861000-87861200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
37	chr6:87861000-87861200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr6:87861000-87861200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr6:87861000-87861200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr6:87861000-87861200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr6:87861000-87861200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
42	chr6:87861000-87861200	Enhancers	Adipose Nuclei	Adipose
43	chr6:87861000-87861200	Enhancers	Liver	Liver
44	chr6:87861000-87861200	Enhancers	Brain Anterior Caudate	brain
45	chr6:87861000-87861200	Flanking Active TSS	Brain Germinal Matrix	brain
46	chr6:87861000-87861200	Enhancers	Colonic Mucosa	Colon
47	chr6:87861000-87861200	Enhancers	Fetal Intestine Large	intestine
48	chr6:87861000-87861200	Enhancers	Fetal Intestine Small	intestine
49	chr6:87861000-87861200	Enhancers	Fetal Kidney	kidney
50	chr6:87861000-87861200	Enhancers	Fetal Muscle Trunk	muscle

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