Variant report

Variant	nsv519218
Chromosome Location	chr6:73845299-73862856
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	ATF2	chr6:73855453-73855770	GM12878	blood:	n/a	n/a
2	BACH1	chr6:73854258-73854268	K562	blood:	n/a	n/a
3	BACH1	chr6:73862435-73862508	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr6:73855406-73855693	GM12878	blood:	n/a	n/a
5	BATF	chr6:73855444-73855746	GM12878	blood:	n/a	n/a
6	CTCF	chr6:73849700-73849850	GM12869	blood:	n/a	n/a
7	E2F4	chr6:73860938-73861197	MCF10A-Er-Src	breast:	n/a	n/a
8	EBF1	chr6:73862345-73862785	GM12878	blood:	n/a	chr6:73862541-73862552
9	EBF1	chr6:73862375-73862726	GM12878	blood:	n/a	chr6:73862541-73862552
10	EBF1	chr6:73862376-73862663	GM12878	blood:	n/a	chr6:73862541-73862552
11	EP300	chr6:73847793-73848087	K562	blood:	n/a	n/a
12	ETS1	chr6:73855304-73855790	GM12878	blood:	n/a	n/a
13	FOS	chr6:73854194-73854269	MCF10A-Er-Src	breast:	n/a	n/a
14	MAFF	chr6:73854165-73854365	K562	blood:	n/a	chr6:73854218-73854236
15	MAFF	chr6:73854124-73854364	HepG2	liver:	n/a	chr6:73854218-73854236
16	MAFK	chr6:73857013-73857074	HepG2	liver:	n/a	chr6:73857023-73857038
17	MAFK	chr6:73854087-73854371	IMR90	lung:	n/a	chr6:73854220-73854235 chr6:73854224-73854238 chr6:73854221-73854241 chr6:73854223-73854239
18	MAFK	chr6:73854060-73854393	HepG2	liver:	n/a	chr6:73854220-73854235 chr6:73854224-73854238 chr6:73854221-73854241 chr6:73854223-73854239
19	MAFK	chr6:73857726-73857972	HepG2	liver:	n/a	chr6:73857825-73857836 chr6:73857823-73857837 chr6:73857820-73857836 chr6:73857824-73857835 chr6:73857825-73857836
20	MAFK	chr6:73854077-73854348	HepG2	liver:	n/a	chr6:73854220-73854235 chr6:73854224-73854238 chr6:73854221-73854241 chr6:73854223-73854239
21	MAX	chr6:73854440-73854634	H1-hESC	embryonic stem cell:	n/a	n/a
22	MAZ	chr6:73853287-73853300	K562	blood:	n/a	n/a
23	MEF2A	chr6:73855382-73855792	GM12878	blood:	n/a	n/a
24	NFIC	chr6:73855427-73855707	GM12878	blood:	n/a	n/a
25	POLR2A	chr6:73861039-73861041	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr6:73849081-73849267	MCF10A-Er-Src	breast:	n/a	n/a
27	POLR2A	chr6:73849797-73849897	GM12878	blood:	n/a	n/a
28	POLR2A	chr6:73861359-73861466	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr6:73848376-73848509	MCF10A-Er-Src	breast:	n/a	n/a
30	POLR2A	chr6:73861500-73861883	H1-neurons	neurons:	n/a	n/a
31	POLR2A	chr6:73861697-73861763	Gliobla	brain:	n/a	n/a
32	RCOR1	chr6:73847789-73847999	K562	blood:	n/a	n/a
33	RUNX3	chr6:73855465-73855771	GM12878	blood:	n/a	n/a
34	RUNX3	chr6:73855425-73855821	GM12878	blood:	n/a	n/a
35	SPI1	chr6:73855426-73855844	GM12891	blood:	n/a	n/a
36	SPI1	chr6:73855523-73855777	GM12878	blood:	n/a	n/a
37	STAT3	chr6:73857345-73857497	MCF10A-Er-Src	breast:	n/a	n/a
38	STAT3	chr6:73854139-73854312	MCF10A-Er-Src	breast:	n/a	chr6:73854264-73854272
39	STAT3	chr6:73861098-73861250	MCF10A-Er-Src	breast:	n/a	n/a
40	STAT3	chr6:73860993-73861075	MCF10A-Er-Src	breast:	n/a	n/a
41	TAL1	chr6:73847785-73848109	K562	blood:	n/a	n/a
42	WRNIP1	chr6:73851977-73852166	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	6:73855086-73857473..6:74078047-74099067	K562	blood:
2	6:73855086-73857473..6:74160392-74184826	K562	blood:
3	6:73859137-73881637..6:74099986-74112890	GM12878	blood:
4	6:73855086-73857473..6:74062967-74076046	GM12878	blood:
5	chr6:73329575..73331858-chr6:73843020..73845929,2	K562	blood:
6	chr6:73846488..73848334-chr6:73855218..73857477,2	K562	blood:
7	6:73859137-73881637..6:73927031-73938730	Hela-S3	cervix:
8	chr6:73843144..73846090-chr6:73848309..73850546,2	K562	blood:
9	chr6:73857256..73859188-chr6:73862622..73864774,2	K562	blood:
10	chr6:73857256..73859188-chr6:73862622..73864774,2	K562	blood:
11	chr6:73843144..73846090-chr6:73848309..73850546,2	K562	blood:
12	chr6:73846488..73848334-chr6:73855218..73857477,2	K562	blood:
13	6:73855086-73857473..6:74099986-74112890	K562	blood:
14	6:73859137-73881637..6:74062967-74076046	GM12878	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-257K9.7.1-1	chr6:73853149-73853237	ENSG00000229154.1
2	lnc-RP11-257K9.7.1-1	chr6:73846356-73846483	ENSG00000229154.1
3	lnc-RP11-257K9.7.1-1	chr6:73851612-73851839	NONHSAT113534
4	lnc-RP11-257K9.7.1-1	chr6:73845817-73845843	NONHSAT113533
5	lnc-RP11-257K9.7.1-1	chr6:73850527-73850680	NONHSAT113532
6	lnc-RP11-257K9.7.1-1	chr6:73846356-73846454	NONHSAT113532
7	lnc-RP11-257K9.7.1-1	chr6:73850527-73850680	NONHSAT113534
8	lnc-RP11-257K9.7.1-1	chr6:73846356-73846454	NONHSAT113534
9	lnc-RP11-257K9.7.1-1	chr6:73853149-73853184	NONHSAT113531
10	lnc-RP11-257K9.7.1-1	chr6:73845290-73845882	ENSG00000229154.1
11	lnc-RP11-257K9.7.1-1	chr6:73851612-73851839	NONHSAT113532

Variant related genes	Relation type
KCNQ5-AS1	TF binding region
ENSG00000203907	chromatin interactions
ENSG00000256980	chromatin interactions
ENSG00000238464	chromatin interactions
ENSG00000203908	chromatin interactions
ENSG00000203909	chromatin interactions
ENSG00000164430	chromatin interactions
ENSG00000224221	chromatin interactions
ENSG00000185760	chromatin interactions
ENSG00000135297	chromatin interactions
ENSG00000207023	chromatin interactions
ENSG00000231332	chromatin interactions
ENSG00000080007	chromatin interactions
ENSG00000235174	chromatin interactions

Extended variants
information (count: 715 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:715 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9446848	chr6:73845299-73845300	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113453470	chr6:73845326-73845327	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs7772526	chr6:73845366-73845367	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs183441393	chr6:73845401-73845402	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs552157306	chr6:73845525-73845526	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs377314140	chr6:73845539-73845540	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs537983120	chr6:73845642-73845643	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs528284288	chr6:73845643-73845644	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs546848344	chr6:73845656-73845657	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs549839735	chr6:73845702-73845703	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs571542743	chr6:73845733-73845734	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs568512804	chr6:73845737-73845738	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs536071644	chr6:73845739-73845740	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs73454729	chr6:73845750-73845751	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs187544158	chr6:73845772-73845773	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs538524080	chr6:73845834-73845835	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs138112960	chr6:73845867-73845868	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs558628397	chr6:73845868-73845869	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs2796051	chr6:73845875-73845876	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs149112665	chr6:73845879-73845880	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs562467811	chr6:73845956-73845957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574440258	chr6:73845984-73845985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191905622	chr6:73846000-73846001	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1418411	chr6:73846002-73846003	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs200019546	chr6:73846010-73846011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs45586535	chr6:73846034-73846035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564166148	chr6:73846045-73846046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531617599	chr6:73846084-73846085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560018001	chr6:73846091-73846092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549728629	chr6:73846105-73846106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528353369	chr6:73846107-73846108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183293574	chr6:73846139-73846140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs16883366	chr6:73846203-73846204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548128737	chr6:73846225-73846226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566653755	chr6:73846226-73846227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2796050	chr6:73846249-73846250	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs116869268	chr6:73846281-73846282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536753116	chr6:73846330-73846331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570732875	chr6:73846465-73846466	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs11753344	chr6:73846469-73846470	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs148303359	chr6:73846497-73846498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556085385	chr6:73846510-73846511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2796049	chr6:73846529-73846530	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs538691250	chr6:73846532-73846533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144854326	chr6:73846557-73846558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188338835	chr6:73846560-73846561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192754747	chr6:73846588-73846589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184113534	chr6:73846641-73846642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2796048	chr6:73846692-73846693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370718782	chr6:73846694-73846695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
Malignant fibrous histiocytomas	21085701	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Breast cancer	20409316	CNVD
Developmental delay	21147756	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:73818000-73846400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:73821000-73849800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr6:73839200-73854400	Weak transcription	Aorta	Aorta
4	chr6:73839800-73852400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr6:73840200-73848000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr6:73840200-73848200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:73840400-73848000	Weak transcription	NHEK	skin
8	chr6:73841400-73846400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr6:73842000-73846200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr6:73842000-73855600	Weak transcription	HSMM	muscle
11	chr6:73843600-73845400	Enhancers	Fetal Lung	lung
12	chr6:73843600-73846000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr6:73843600-73846400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr6:73844400-73845800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr6:73844400-73867000	Weak transcription	Primary hematopoietic stem cells	blood
16	chr6:73844600-73845400	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr6:73844600-73847600	Weak transcription	GM12878-XiMat	blood
18	chr6:73844600-73849800	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr6:73844600-73865200	Weak transcription	Primary T cells from cord blood	blood
20	chr6:73844800-73846800	Weak transcription	NHLF	lung
21	chr6:73844800-73866400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr6:73845000-73846400	Strong transcription	Primary B cells from cord blood	blood
23	chr6:73845400-73847800	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr6:73846000-73866400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr6:73846400-73847800	Weak transcription	Primary B cells from cord blood	blood
26	chr6:73846400-73847800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr6:73846400-73879200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:73847800-73848000	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr6:73847800-73848600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
30	chr6:73847800-73850600	Strong transcription	Primary B cells from cord blood	blood
31	chr6:73848000-73848400	Enhancers	NHEK	skin
32	chr6:73848000-73848600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr6:73848200-73848400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr6:73848200-73848600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr6:73848400-73848800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr6:73848600-73849800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr6:73849800-73850800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
38	chr6:73850600-73851600	Weak transcription	Primary B cells from cord blood	blood
39	chr6:73850800-73853000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr6:73851600-73852800	Strong transcription	Primary B cells from cord blood	blood
41	chr6:73852800-73854400	Weak transcription	Primary B cells from cord blood	blood
42	chr6:73853000-73856200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
43	chr6:73853600-73854200	Weak transcription	GM12878-XiMat	blood
44	chr6:73854200-73854400	ZNF genes & repeats	GM12878-XiMat	blood
45	chr6:73854400-73854600	ZNF genes & repeats	Aorta	Aorta
46	chr6:73854400-73854600	Enhancers	Esophagus	oesophagus
47	chr6:73854400-73854600	Enhancers	GM12878-XiMat	blood
48	chr6:73854400-73854800	Enhancers	Brain Anterior Caudate	brain
49	chr6:73854400-73856600	Strong transcription	Primary B cells from cord blood	blood
50	chr6:73854600-73854800	ZNF genes & repeats	GM12878-XiMat	blood

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