Variant report

Variant	nsv886141
Chromosome Location	chr6:70590638-70694162
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:672)
CpG islands
(count:0)
Chromatin interactive
region (count:26)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:70640798-70640916	K562	blood:	n/a	n/a
2	ATF1	chr6:70628051-70628170	K562	blood:	n/a	n/a
3	ATF1	chr6:70684183-70684412	K562	blood:	n/a	n/a
4	ATF2	chr6:70596859-70597496	GM12878	blood:	n/a	n/a
5	ATF2	chr6:70591129-70592202	GM12878	blood:	n/a	n/a
6	ATF2	chr6:70604532-70605363	GM12878	blood:	n/a	n/a
7	ATF2	chr6:70591103-70592149	GM12878	blood:	n/a	n/a
8	ATF2	chr6:70604541-70605386	GM12878	blood:	n/a	n/a
9	BACH1	chr6:70633640-70633675	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr6:70604539-70604766	GM12878	blood:	n/a	n/a
11	BATF	chr6:70636666-70636908	GM12878	blood:	n/a	chr6:70636798-70636809
12	BATF	chr6:70591680-70591949	GM12878	blood:	n/a	n/a
13	BATF	chr6:70605083-70605425	GM12878	blood:	n/a	n/a
14	BATF	chr6:70636711-70636885	GM12878	blood:	n/a	chr6:70636798-70636809
15	BCL11A	chr6:70604483-70604808	GM12878	blood:	n/a	n/a
16	BCL11A	chr6:70604448-70604793	GM12878	blood:	n/a	n/a
17	BCL11A	chr6:70591669-70592020	GM12878	blood:	n/a	n/a
18	BCL11A	chr6:70591684-70592024	GM12878	blood:	n/a	n/a
19	BCL3	chr6:70591685-70592018	GM12878	blood:	n/a	n/a
20	BCLAF1	chr6:70591154-70592039	GM12878	blood:	n/a	chr6:70591409-70591418
21	BCLAF1	chr6:70604460-70604844	GM12878	blood:	n/a	n/a
22	BCLAF1	chr6:70604828-70605391	GM12878	blood:	n/a	n/a
23	BCLAF1	chr6:70591580-70592040	GM12878	blood:	n/a	n/a
24	BHLHE40	chr6:70675582-70675731	K562	blood:	n/a	n/a
25	BHLHE40	chr6:70590475-70592324	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:70604549-70605325	GM12878	blood:	n/a	n/a
27	BHLHE40	chr6:70623359-70623456	GM12878	blood:	n/a	n/a
28	BHLHE40	chr6:70596967-70597398	GM12878	blood:	n/a	n/a
29	CCNT2	chr6:70633639-70633865	K562	blood:	n/a	n/a
30	CEBPB	chr6:70646522-70646896	IMR90	lung:	n/a	chr6:70646702-70646713
31	CEBPB	chr6:70640688-70641006	HepG2	liver:	n/a	chr6:70640863-70640876 chr6:70640864-70640875 chr6:70640863-70640876
32	CEBPB	chr6:70604484-70604903	MCF-7	breast:	n/a	n/a
33	CEBPB	chr6:70646475-70646926	ECC-1	luminal epithelium:	n/a	chr6:70646702-70646713
34	CEBPB	chr6:70640708-70641022	IMR90	lung:	n/a	chr6:70640863-70640876 chr6:70640864-70640875 chr6:70640863-70640876
35	CEBPB	chr6:70680894-70681234	IMR90	lung:	n/a	n/a
36	CEBPB	chr6:70646570-70646862	H1-hESC	embryonic stem cell:	n/a	chr6:70646702-70646713
37	CEBPB	chr6:70646523-70646886	K562	blood:	n/a	chr6:70646702-70646713
38	CEBPB	chr6:70684148-70684405	K562	blood:	n/a	chr6:70684257-70684268
39	CEBPB	chr6:70604460-70604852	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr6:70640709-70640987	K562	blood:	n/a	chr6:70640863-70640876 chr6:70640864-70640875 chr6:70640863-70640876
41	CEBPB	chr6:70646521-70646883	Hela-S3	cervix:	n/a	chr6:70646702-70646713
42	CEBPB	chr6:70684061-70684468	MCF-7	breast:	n/a	chr6:70684257-70684268
43	CEBPB	chr6:70625364-70625604	HepG2	liver:	n/a	chr6:70625475-70625488 chr6:70625475-70625486 chr6:70625477-70625488
44	CEBPB	chr6:70646534-70646894	HepG2	liver:	n/a	chr6:70646702-70646713
45	CEBPB	chr6:70646556-70646882	A549	lung:	n/a	chr6:70646702-70646713
46	CEBPB	chr6:70683651-70683904	HepG2	liver:	n/a	chr6:70683750-70683761
47	CEBPB	chr6:70640771-70641000	A549	lung:	n/a	chr6:70640863-70640876 chr6:70640864-70640875 chr6:70640863-70640876
48	CEBPB	chr6:70642621-70642881	IMR90	lung:	n/a	n/a
49	CEBPB	chr6:70627684-70628222	IMR90	lung:	n/a	n/a
50	CEBPB	chr6:70689950-70690228	K562	blood:	n/a	chr6:70690098-70690109

No data

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:70680703..70682726-chr6:70685209..70687558,2	K562	blood:
2	chr6:70637494..70639409-chr6:70659032..70661217,2	K562	blood:
3	chr6:70656949..70658468-chr6:70663252..70666166,2	K562	blood:
4	chr6:70624667..70626403-chr6:70626654..70628205,2	K562	blood:
5	chr6:70664026..70665656-chr6:70667734..70669345,2	K562	blood:
6	chr6:70662410..70664369-chr6:70665696..70668642,2	K562	blood:
7	chr6:70637494..70639409-chr6:70659032..70661217,2	K562	blood:
8	chr6:70604781..70606444-chr6:70609800..70611681,2	MCF-7	breast:
9	chr6:70661572..70663140-chr6:70670607..70672802,2	MCF-7	breast:
10	chr6:70669047..70671933-chr6:70674110..70676745,3	MCF-7	breast:
11	chr6:70664026..70665656-chr6:70667734..70669345,2	K562	blood:
12	chr6:70669047..70671933-chr6:70674110..70676745,3	MCF-7	breast:
13	chr6:70589300..70592044-chr6:70621641..70624143,2	K562	blood:
14	chr6:70646120..70647757-chr6:70648588..70650873,2	MCF-7	breast:
15	chr6:70661572..70663140-chr6:70670607..70672802,2	MCF-7	breast:
16	chr6:70624667..70626403-chr6:70626654..70628205,2	K562	blood:
17	chr6:70637673..70640119-chr6:70644404..70646417,2	K562	blood:
18	chr6:70604781..70606444-chr6:70609800..70611681,2	MCF-7	breast:
19	chr6:70656949..70658468-chr6:70663252..70666166,2	K562	blood:
20	chr6:70589300..70592044-chr6:70621641..70624143,2	K562	blood:
21	chr6:70637673..70640119-chr6:70644404..70646417,2	K562	blood:
22	chr6:70683823..70685555-chr6:70687830..70690193,2	K562	blood:
23	chr6:70662410..70664369-chr6:70665696..70668642,2	K562	blood:
24	chr6:70680703..70682726-chr6:70685209..70687558,2	K562	blood:
25	chr6:70584342..70586150-chr6:70590022..70592007,2	K562	blood:
26	chr6:70683823..70685555-chr6:70687830..70690193,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAI3-5	chr6:70599810-70601112	NONHSAT113425
2	lnc-FAM135A-5	chr6:70646764-70646802	NONHSAT113426
3	lnc-FAM135A-5	chr6:70647930-70647992	NONHSAT113426
4	lnc-FAM135A-5	chr6:70683731-70684088	NONHSAT113426
5	lnc-FAM135A-5	chr6:70669888-70669932	NONHSAT113426
6	lnc-FAM135A-5	chr6:70672718-70672762	NONHSAT113426

No data

Variant related genes	Relation type
COL19A1	TF binding region
ENSG00000082293	chromatin interactions

Extended variants
information (count: 3603 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3603 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12201139	chr6:70590638-70590639	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531084043	chr6:70590642-70590643	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs192953859	chr6:70590662-70590663	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs570836981	chr6:70590718-70590719	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs146988472	chr6:70590745-70590746	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs553493912	chr6:70590746-70590747	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs566927895	chr6:70590957-70590958	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs184119774	chr6:70590983-70590984	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs555241710	chr6:70590999-70591000	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs138193987	chr6:70591034-70591035	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs544165226	chr6:70591122-70591123	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs557765971	chr6:70591159-70591160	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs577217627	chr6:70591167-70591168	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs539982439	chr6:70591174-70591175	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs143761517	chr6:70591176-70591177	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs572995729	chr6:70591186-70591187	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs73749319	chr6:70591265-70591266	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs72004207	chr6:70591303-70591304	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558176113	chr6:70591305-70591306	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542431301	chr6:70591315-70591316	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs12189777	chr6:70591331-70591332	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs543122118	chr6:70591333-70591334	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368028028	chr6:70591344-70591345	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561313045	chr6:70591372-70591373	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs35341858	chr6:70591446-70591447	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573323390	chr6:70591450-70591451	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113670713	chr6:70591453-70591454	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550987793	chr6:70591460-70591461	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189499143	chr6:70591464-70591465	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533374928	chr6:70591477-70591478	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546966622	chr6:70591483-70591484	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143237423	chr6:70591518-70591519	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535542695	chr6:70591552-70591553	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192491469	chr6:70591575-70591576	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73478063	chr6:70591602-70591603	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs184903934	chr6:70591639-70591640	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs141420549	chr6:70591652-70591653	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs957316	chr6:70591721-70591722	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs533548131	chr6:70591736-70591737	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs148813414	chr6:70591770-70591771	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs73478064	chr6:70591790-70591791	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs573419053	chr6:70591800-70591801	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs542335257	chr6:70591840-70591841	Weak transcription Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562352501	chr6:70591845-70591846	Weak transcription Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs189578964	chr6:70591871-70591872	Weak transcription Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540661729	chr6:70591876-70591877	Weak transcription Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs150838862	chr6:70591878-70591879	Weak transcription Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs544750584	chr6:70591880-70591881	Weak transcription Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs564770700	chr6:70591881-70591882	Weak transcription Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs533637584	chr6:70591942-70591943	Weak transcription Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Gastrointestinal stromal cancer	20818650	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
Developmental delay	21147756	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
Cancer	20164919	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	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:396 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70578600-70591600	Weak transcription	Fetal Heart	heart
2	chr6:70588800-70597800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:70589600-70591800	Flanking Active TSS	Primary B cells from cord blood	blood
4	chr6:70590600-70590800	Enhancers	Primary B cells from peripheral blood	blood
5	chr6:70590600-70592200	Active TSS	GM12878-XiMat	blood
6	chr6:70590800-70591200	Flanking Active TSS	Primary B cells from peripheral blood	blood
7	chr6:70590800-70592000	Enhancers	Fetal Lung	lung
8	chr6:70591200-70591600	Active TSS	Primary B cells from peripheral blood	blood
9	chr6:70591400-70592000	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr6:70591400-70592200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr6:70591400-70592400	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr6:70591600-70591800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:70591600-70591800	Flanking Active TSS	Primary B cells from peripheral blood	blood
14	chr6:70591600-70591800	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
15	chr6:70591600-70591800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr6:70591600-70593400	Enhancers	Fetal Heart	heart
17	chr6:70591800-70592000	Active TSS	Primary B cells from peripheral blood	blood
18	chr6:70591800-70592000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr6:70591800-70592000	Enhancers	Psoas Muscle	Psoas
20	chr6:70591800-70592400	Active TSS	Primary B cells from cord blood	blood
21	chr6:70591800-70592600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr6:70591800-70592600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
23	chr6:70592000-70592400	Flanking Active TSS	Primary B cells from peripheral blood	blood
24	chr6:70592000-70593000	Weak transcription	Psoas Muscle	Psoas
25	chr6:70592200-70592400	Flanking Active TSS	GM12878-XiMat	blood
26	chr6:70592400-70592600	Flanking Active TSS	Primary B cells from cord blood	blood
27	chr6:70592400-70592800	Enhancers	GM12878-XiMat	blood
28	chr6:70592400-70595200	Enhancers	Primary B cells from peripheral blood	blood
29	chr6:70592600-70593200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr6:70592600-70594800	Enhancers	Primary B cells from cord blood	blood
31	chr6:70592800-70593000	Flanking Active TSS	GM12878-XiMat	blood
32	chr6:70592800-70593200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr6:70593000-70593200	Genic enhancers	GM12878-XiMat	blood
34	chr6:70593000-70593400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr6:70593000-70593400	Enhancers	Left Ventricle	heart
36	chr6:70593000-70593400	Enhancers	Psoas Muscle	Psoas
37	chr6:70593000-70593400	Enhancers	Right Atrium	heart
38	chr6:70593200-70593400	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
39	chr6:70593200-70594400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:70593200-70597600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr6:70593400-70593800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr6:70593400-70593800	Genic enhancers	GM12878-XiMat	blood
43	chr6:70593800-70594200	Weak transcription	GM12878-XiMat	blood
44	chr6:70594200-70597000	ZNF genes & repeats	GM12878-XiMat	blood
45	chr6:70594400-70594600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr6:70594600-70595400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr6:70594800-70595400	Weak transcription	Primary B cells from cord blood	blood
48	chr6:70595200-70595400	Weak transcription	Primary B cells from peripheral blood	blood
49	chr6:70595400-70596200	Strong transcription	Primary B cells from peripheral blood	blood
50	chr6:70595400-70596400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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