Variant report

Variant	nsv441702
Chromosome Location	chr6:134550755-134557203
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	ATF1	chr6:134557149-134557476	K562	blood:	n/a	n/a
2	ATF2	chr6:134556934-134557658	GM12878	blood:	n/a	n/a
3	ATF2	chr6:134556974-134557702	GM12878	blood:	n/a	n/a
4	ATF3	chr6:134557100-134557443	K562	blood:	n/a	n/a
5	BATF	chr6:134557102-134557605	GM12878	blood:	n/a	chr6:134557370-134557380 chr6:134557369-134557380
6	BCL11A	chr6:134557052-134557618	GM12878	blood:	n/a	chr6:134557408-134557417 chr6:134557119-134557128 chr6:134557369-134557378
7	BCL3	chr6:134557088-134557576	GM12878	blood:	n/a	chr6:134557408-134557417 chr6:134557119-134557128 chr6:134557369-134557378
8	BCLAF1	chr6:134556901-134557695	GM12878	blood:	n/a	chr6:134557408-134557417 chr6:134557119-134557128 chr6:134557369-134557378
9	BHLHE40	chr6:134556983-134557701	K562	blood:	n/a	n/a
10	BHLHE40	chr6:134556946-134557773	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:134556243-134556438	GM12878	blood:	n/a	n/a
12	CEBPB	chr6:134554405-134554613	HepG2	liver:	n/a	chr6:134554492-134554505 chr6:134554444-134554455
13	CEBPB	chr6:134555864-134556031	K562	blood:	n/a	n/a
14	CEBPB	chr6:134552163-134552392	IMR90	lung:	n/a	n/a
15	CEBPB	chr6:134554334-134554862	HepG2	liver:	n/a	chr6:134554492-134554505 chr6:134554444-134554455
16	CEBPB	chr6:134556916-134557770	GM12878	blood:	n/a	n/a
17	CEBPB	chr6:134554373-134554640	K562	blood:	n/a	chr6:134554492-134554505 chr6:134554444-134554455
18	CEBPB	chr6:134555889-134556080	K562	blood:	n/a	n/a
19	CEBPB	chr6:134557164-134557458	GM12878	blood:	n/a	n/a
20	CHD2	chr6:134557168-134557594	GM12878	blood:	n/a	n/a
21	CREB1	chr6:134557045-134557570	GM12878	blood:	n/a	n/a
22	CREB1	chr6:134557059-134557712	GM12878	blood:	n/a	n/a
23	CUX1	chr6:134557054-134557599	GM12878	blood:	n/a	n/a
24	E2F4	chr6:134557150-134557443	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr6:134556150-134556319	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F6	chr6:134557008-134557272	K562	blood:	n/a	n/a
27	EBF1	chr6:134557099-134557544	GM12878	blood:	n/a	n/a
28	ELK1	chr6:134557120-134557528	GM12878	blood:	n/a	n/a
29	EP300	chr6:134557132-134557472	K562	blood:	n/a	chr6:134557369-134557378 chr6:134557341-134557355
30	EP300	chr6:134557132-134557587	GM12878	blood:	n/a	chr6:134557369-134557378 chr6:134557341-134557355
31	EP300	chr6:134557059-134557513	HepG2	liver:	n/a	chr6:134557369-134557378 chr6:134557341-134557355
32	EP300	chr6:134557123-134557635	GM12878	blood:	n/a	chr6:134557369-134557378 chr6:134557341-134557355
33	EP300	chr6:134557030-134557698	GM12878	blood:	n/a	chr6:134557369-134557378 chr6:134557341-134557355
34	FOS	chr6:134557133-134557544	MCF10A-Er-Src	breast:	n/a	chr6:134557291-134557302 chr6:134557367-134557378 chr6:134557369-134557377 chr6:134557295-134557303 chr6:134557369-134557376 chr6:134557369-134557377
35	FOS	chr6:134557105-134557860	MCF10A-Er-Src	breast:	n/a	chr6:134557291-134557302 chr6:134557367-134557378 chr6:134557369-134557377 chr6:134557295-134557303 chr6:134557369-134557376 chr6:134557369-134557377
36	FOS	chr6:134557130-134557988	MCF10A-Er-Src	breast:	n/a	chr6:134557291-134557302 chr6:134557367-134557378 chr6:134557369-134557377 chr6:134557295-134557303 chr6:134557369-134557376 chr6:134557369-134557377
37	FOS	chr6:134557130-134558005	MCF10A-Er-Src	breast:	n/a	chr6:134557291-134557302 chr6:134557367-134557378 chr6:134557369-134557377 chr6:134557295-134557303 chr6:134557369-134557376 chr6:134557369-134557377
38	FOS	chr6:134551377-134551667	HUVEC	blood vessel:	n/a	n/a
39	FOS	chr6:134557087-134557549	HUVEC	blood vessel:	n/a	chr6:134557291-134557302 chr6:134557367-134557378 chr6:134557369-134557377 chr6:134557295-134557303 chr6:134557369-134557376 chr6:134557369-134557377
40	FOSL1	chr6:134557182-134557562	HCT-116	colon:	n/a	chr6:134557291-134557302 chr6:134557369-134557377 chr6:134557295-134557303 chr6:134557369-134557376 chr6:134557369-134557377
41	FOSL2	chr6:134557162-134557573	HepG2	liver:	n/a	chr6:134557366-134557377 chr6:134557291-134557302 chr6:134557369-134557377 chr6:134557295-134557303 chr6:134557369-134557376 chr6:134557369-134557377
42	FOSL2	chr6:134557025-134557602	SK-N-SH	brain:	n/a	chr6:134557366-134557377 chr6:134557291-134557302 chr6:134557369-134557377 chr6:134557295-134557303 chr6:134557369-134557376 chr6:134557369-134557377
43	FOSL2	chr6:134557057-134557510	A549	lung:	n/a	chr6:134557366-134557377 chr6:134557291-134557302 chr6:134557369-134557377 chr6:134557295-134557303 chr6:134557369-134557376 chr6:134557369-134557377
44	FOSL2	chr6:134557182-134557564	HepG2	liver:	n/a	chr6:134557366-134557377 chr6:134557291-134557302 chr6:134557369-134557377 chr6:134557295-134557303 chr6:134557369-134557376 chr6:134557369-134557377
45	FOXM1	chr6:134556986-134557674	GM12878	blood:	n/a	n/a
46	FOXM1	chr6:134556920-134557680	GM12878	blood:	n/a	n/a
47	FOXP2	chr6:134551494-134551681	PFSK-1	brain:	n/a	n/a
48	JUN	chr6:134557120-134557514	K562	blood:	n/a	chr6:134557291-134557302 chr6:134557369-134557377 chr6:134557295-134557303 chr6:134557369-134557376 chr6:134557369-134557377
49	JUN	chr6:134557134-134557517	K562	blood:	n/a	chr6:134557291-134557302 chr6:134557369-134557377 chr6:134557295-134557303 chr6:134557369-134557376 chr6:134557369-134557377
50	JUN	chr6:134557027-134557512	K562	blood:	n/a	chr6:134557291-134557302 chr6:134557369-134557377 chr6:134557295-134557303 chr6:134557369-134557376 chr6:134557369-134557377

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:134553108..134554693-chr6:134556354..134559341,2	MCF-7	breast:
2	chr6:134553108..134554693-chr6:134556354..134559341,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC2A12-8	chr6:134551538-134551619	NONHSAT115023

Variant related genes	Relation type
SGK1	TF binding region

Extended variants
information (count: 201 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:201 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9376018	chr6:134550758-134550759	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs57109798	chr6:134550761-134550762	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs139015663	chr6:134550788-134550789	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567185123	chr6:134550821-134550822	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543977049	chr6:134550841-134550842	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376795452	chr6:134550861-134550862	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373959938	chr6:134550866-134550867	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570174722	chr6:134550879-134550880	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552671264	chr6:134550900-134550901	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560730323	chr6:134550978-134550979	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs57030520	chr6:134550981-134550982	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200699518	chr6:134551004-134551005	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs58598912	chr6:134551057-134551058	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs558766782	chr6:134551128-134551129	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551974936	chr6:134551137-134551138	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563352834	chr6:134551181-134551182	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568978769	chr6:134551187-134551188	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112257073	chr6:134551192-134551193	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146186550	chr6:134551306-134551307	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs540588696	chr6:134551338-134551339	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs560580242	chr6:134551406-134551407	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs532696918	chr6:134551459-134551460	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs530481655	chr6:134551481-134551482	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs1743947	chr6:134551547-134551548	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs530716504	chr6:134551654-134551655	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs532089217	chr6:134551669-134551670	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs55997806	chr6:134551721-134551722	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs397779199	chr6:134551728-134551729	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs199525489	chr6:134551729-134551730	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs367743992	chr6:134551755-134551756	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs550616955	chr6:134551824-134551825	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs567526028	chr6:134551855-134551856	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs6569935	chr6:134551910-134551911	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs546147878	chr6:134551917-134551918	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs56263564	chr6:134551928-134551929	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs111469853	chr6:134552013-134552014	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs7770989	chr6:134552022-134552023	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs142164300	chr6:134552060-134552061	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs538398779	chr6:134552071-134552072	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs554968166	chr6:134552083-134552084	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs186779508	chr6:134552088-134552089	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs540920722	chr6:134552103-134552104	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs151229242	chr6:134552144-134552145	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs566338486	chr6:134552200-134552201	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs116288914	chr6:134552201-134552202	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs546354091	chr6:134552225-134552226	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs530344573	chr6:134552226-134552227	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs192651388	chr6:134552255-134552256	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs12206857	chr6:134552309-134552310	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs1743946	chr6:134552345-134552346	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:88)

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
Autism	22495311	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
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	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
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:147 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:134532800-134551200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr6:134536400-134551600	Weak transcription	Primary T cells from cord blood	blood
3	chr6:134545200-134551200	Weak transcription	Adipose Nuclei	Adipose
4	chr6:134545600-134550800	Weak transcription	Brain Anterior Caudate	brain
5	chr6:134545600-134550800	Weak transcription	Brain Hippocampus Middle	brain
6	chr6:134545800-134554600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr6:134547800-134557600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:134549600-134551600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr6:134550200-134551000	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr6:134550200-134551800	Enhancers	H1 Cell Line	embryonic stem cell
11	chr6:134550400-134551000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr6:134550400-134551400	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr6:134550400-134551600	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr6:134550400-134552200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
15	chr6:134550600-134551200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr6:134550600-134551200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr6:134550600-134551200	Active TSS	Primary hematopoietic stem cells	blood
18	chr6:134550600-134551200	Active TSS	Duodenum Mucosa	Duodenum
19	chr6:134550600-134551400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr6:134550600-134551400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
21	chr6:134550600-134551600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr6:134550600-134551600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr6:134550600-134551800	Flanking Active TSS	Primary B cells from cord blood	blood
24	chr6:134550600-134551800	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr6:134550600-134552400	Enhancers	Primary B cells from peripheral blood	blood
26	chr6:134550800-134551000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr6:134550800-134551200	Enhancers	GM12878-XiMat	blood
28	chr6:134550800-134551400	Enhancers	Brain Anterior Caudate	brain
29	chr6:134550800-134551600	Flanking Active TSS	Brain Hippocampus Middle	brain
30	chr6:134550800-134551800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr6:134550800-134552000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr6:134550800-134552400	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr6:134550800-134552400	Enhancers	Fetal Thymus	thymus
34	chr6:134551000-134551400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
35	chr6:134551000-134564000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr6:134551200-134551400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr6:134551200-134551400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
38	chr6:134551200-134551400	Enhancers	Adipose Nuclei	Adipose
39	chr6:134551200-134551400	Flanking Active TSS	GM12878-XiMat	blood
40	chr6:134551200-134551600	Flanking Active TSS	Primary hematopoietic stem cells	blood
41	chr6:134551200-134551600	Active TSS	Rectal Mucosa Donor 29	rectum
42	chr6:134551200-134551800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr6:134551200-134551800	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr6:134551200-134551800	Enhancers	HUVEC	blood vessel
45	chr6:134551400-134551600	Enhancers	GM12878-XiMat	blood
46	chr6:134551400-134552800	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr6:134551400-134554200	Weak transcription	Brain Anterior Caudate	brain
48	chr6:134551400-134558800	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr6:134551400-134559600	Weak transcription	Adipose Nuclei	Adipose
50	chr6:134551400-134560200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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