Variant report

Variant	esv16232
Chromosome Location	chr6:167609519-167781943
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2701)
CpG islands
(count:4335)
Chromatin interactive
region (count:33)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2701 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167633428-167633974	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167629415-167629646	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167682223-167682912	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167652605-167653007	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:167628930-167629130	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:167632046-167632420	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:167655013-167655211	HepG2	liver:	n/a	n/a
13	ARID3A	chr6:167629887-167630151	HepG2	liver:	n/a	n/a
14	ARID3A	chr6:167624462-167624811	HepG2	liver:	n/a	n/a
15	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
16	ARID3A	chr6:167637599-167638030	HepG2	liver:	n/a	n/a
17	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
18	ARID3A	chr6:167645950-167646149	HepG2	liver:	n/a	n/a
19	ARID3A	chr6:167651727-167651738	HepG2	liver:	n/a	n/a
20	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
21	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
22	ATF2	chr6:167651500-167652487	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr6:167641353-167641826	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr6:167641333-167641936	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr6:167625939-167626508	GM12878	blood:	n/a	n/a
26	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr6:167626020-167626431	GM12878	blood:	n/a	n/a
29	BACH1	chr6:167637370-167637829	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:167631950-167632087	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr6:167641591-167641850	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr6:167702257-167702472	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
35	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
36	BATF	chr6:167625959-167626402	GM12878	blood:	n/a	n/a
37	BATF	chr6:167631870-167632155	GM12878	blood:	n/a	n/a
38	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
39	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
40	BATF	chr6:167702166-167702414	GM12878	blood:	n/a	n/a
41	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
42	BATF	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
43	BATF	chr6:167625794-167626502	GM12878	blood:	n/a	n/a
44	BCL11A	chr6:167626130-167626424	GM12878	blood:	n/a	n/a
45	BCL3	chr6:167710341-167710705	GM12878	blood:	n/a	n/a
46	BCLAF1	chr6:167764829-167765189	GM12878	blood:	n/a	chr6:167764879-167764888 chr6:167765036-167765044
47	BHLHE40	chr6:167722070-167722725	HepG2	liver:	n/a	chr6:167722523-167722539
48	BHLHE40	chr6:167617588-167617796	HepG2	liver:	n/a	n/a
49	BHLHE40	chr6:167617544-167617803	K562	blood:	n/a	n/a
50	BHLHE40	chr6:167699851-167700081	HepG2	liver:	n/a	n/a

(count:4335 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167764146-167764196	HCPEpiC	choroid plexus:	n/a
2	chr6:167764967-167765017	SK-N-MC	brain:	n/a
3	chr6:167649539-167649589	NHDF-neo	bronchial:	n/a
4	chr6:167653957-167654007	AG10803	skin:	n/a
5	chr6:167764146-167764196	HCPEpiC	choroid plexus:	n/a
6	chr6:167764967-167765017	SK-N-MC	brain:	n/a
7	chr6:167649539-167649589	NHDF-neo	bronchial:	n/a
8	chr6:167653957-167654007	AG10803	skin:	n/a
9	chr6:167616968-167617018	PFSK-1	brain:	n/a
10	chr6:167635072-167635122	SK-N-SH	brain:	n/a
11	chr6:167649631-167649681	SKMC	muscle:	n/a
12	chr6:167649631-167649681	HCM	heart:	n/a
13	chr6:167709720-167709770	AG04449	skin:	fetal
14	chr6:167649631-167649681	HUVEC	blood vessel:	n/a
15	chr6:167756099-167756149	NHDF-neo	bronchial:	n/a
16	chr6:167765215-167765265	NHBE	bronchial:	n/a
17	chr6:167765215-167765265	HCPEpiC	choroid plexus:	n/a
18	chr6:167738277-167738327	CMK	blood:	n/a
19	chr6:167761204-167761254	NHDF-neo	bronchial:	n/a
20	chr6:167680447-167680497	HCPEpiC	choroid plexus:	n/a
21	chr6:167635072-167635122	AoSMC	blood vessel:	n/a
22	chr6:167762783-167762833	HCM	heart:	n/a
23	chr6:167763758-167763808	U87	brain:	n/a
24	chr6:167704769-167704819	HCPEpiC	choroid plexus:	n/a
25	chr6:167738342-167738392	GM12891	blood:	n/a
26	chr6:167734054-167734104	Caco-2	colon:	n/a
27	chr6:167655053-167655103	PFSK-1	brain:	n/a
28	chr6:167700000-167700050	AoSMC	blood vessel:	n/a
29	chr6:167703894-167703944	BE2_C	brain:	n/a
30	chr6:167765215-167765265	LNCaP	prostate:	n/a
31	chr6:167617119-167617169	HCPEpiC	choroid plexus:	n/a
32	chr6:167653907-167653957	ovcar-3	ovarian:	n/a
33	chr6:167734054-167734104	HCPEpiC	choroid plexus:	n/a
34	chr6:167655290-167655340	HepG2	liver:	n/a
35	chr6:167649749-167649799	NB4	blood:	n/a
36	chr6:167709237-167709287	BE2_C	brain:	n/a
37	chr6:167761204-167761254	K562	blood:	n/a
38	chr6:167708827-167708877	HCM	heart:	n/a
39	chr6:167761204-167761254	AG04449	skin:	fetal
40	chr6:167654977-167655027	HCPEpiC	choroid plexus:	n/a
41	chr6:167705253-167705303	HepG2	liver:	n/a
42	chr6:167761204-167761254	U87	brain:	n/a
43	chr6:167649336-167649386	HIPEpiC	eye:	n/a
44	chr6:167763320-167763370	Hepatocyte	liver:	n/a
45	chr6:167704808-167704858	ProgFib	skin:	n/a
46	chr6:167703591-167703641	HRPEpiC	eye:	n/a
47	chr6:167763819-167763869	HCPEpiC	choroid plexus:	n/a
48	chr6:167763758-167763808	GM12891	blood:	n/a
49	chr6:167738592-167738642	PFSK-1	brain:	n/a
50	chr6:167661905-167661955	HRPEpiC	eye:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
2	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
3	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
4	chr1:28836187..28837925-chr6:167694572..167696254,2	K562	blood:
5	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
6	chr6:167699179..167702166-chr6:167703091..167705361,2	K562	blood:
7	chr6:167669951..167671777-chr6:167683631..167687000,3	K562	blood:
8	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
9	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
10	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
11	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
12	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
13	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
14	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
15	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
16	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
17	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
18	chr6:167668192..167671777-chr6:167684157..167687082,3	K562	blood:
19	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
20	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
21	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
22	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
23	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
24	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
25	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
26	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
27	chr6:167703616..167705764-chr6:167717598..167719278,2	MCF-7	breast:
28	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
29	chr6:167623945..167626187-chr6:168297648..168300373,2	K562	blood:
30	chr6:167620399..167623068-chr6:167623897..167626646,2	K562	blood:
31	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
32	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
33	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR31-1	chr6:167650996-167651293	XLOC_005921
2	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095
3	lnc-UNC93A-1	chr6:167659275-167659404	XLOC_005540
4	lnc-UNC93A-3	chr6:167764293-167764966	NONHSAT116095
5	lnc-UNC93A-1	chr6:167655379-167655453	XLOC_005540
6	lnc-GPR31-1	chr6:167653688-167653968	XLOC_005921
7	lnc-GPR31-1	chr6:167651156-167651293	XLOC_005921
8	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094
9	lnc-GPR31-1	chr6:167653636-167653833	XLOC_005921

No data

Variant related genes	Relation type
UNC93A	TF binding region
ENSG00000228648	TF binding region
TTLL2	TF binding region
ENSG00000231720	TF binding region
ENSG00000216966	TF binding region
ENSG00000217447	TF binding region
UNC93A	CpG island
ENSG00000228648	CpG island
TTLL2	CpG island
ENSG00000231720	CpG island
ENSG00000216966	CpG island
ENSG00000217447	CpG island
ENSG00000180198	chromatin interactions
ENSG00000216966	chromatin interactions
ENSG00000112494	chromatin interactions
CYB5R4	miRNA target sites
CYBASC3	miRNA target sites

Extended variants
information (count: 8470 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:8470 , 50 per page) page: 1 2 3 4 5 6 7 ... 170

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75159046	chr6:167609528-167609529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537095771	chr6:167609558-167609559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558695537	chr6:167609560-167609561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570601644	chr6:167609561-167609562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534312422	chr6:167609565-167609566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375663776	chr6:167609566-167609567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7770917	chr6:167609567-167609568	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs575063863	chr6:167609613-167609614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542176200	chr6:167609626-167609627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs760617	chr6:167609643-167609644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs557505398	chr6:167609658-167609659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs575755777	chr6:167609660-167609661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2077083	chr6:167609691-167609692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs141837572	chr6:167609708-167609709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs377204765	chr6:167609731-167609732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs144542538	chr6:167609817-167609818	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs546025035	chr6:167609840-167609841	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs564235754	chr6:167609841-167609842	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs573027512	chr6:167609844-167609845	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs540215099	chr6:167609864-167609865	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs561953262	chr6:167609938-167609939	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs200999685	chr6:167609989-167609990	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs529972331	chr6:167610034-167610035	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs548191391	chr6:167610056-167610057	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs376434672	chr6:167610065-167610066	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs530715919	chr6:167610133-167610134	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs552447314	chr6:167610137-167610138	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs570540893	chr6:167610328-167610329	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs760615	chr6:167610336-167610337	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs534744803	chr6:167610344-167610345	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs546543082	chr6:167610367-167610368	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs2345797	chr6:167610371-167610372	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs2345798	chr6:167610380-167610381	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs536116090	chr6:167610398-167610399	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs374161953	chr6:167610407-167610408	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs35402603	chr6:167610487-167610488	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs557358359	chr6:167610501-167610502	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs575564112	chr6:167610533-167610534	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs138586830	chr6:167610550-167610551	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs148851725	chr6:167610656-167610657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs572963154	chr6:167610717-167610718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs143477035	chr6:167610726-167610727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs562086667	chr6:167610803-167610804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538015062	chr6:167610815-167610816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs6456163	chr6:167610819-167610820	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs137892339	chr6:167610836-167610837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7762000	chr6:167610865-167610866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs116615659	chr6:167610892-167610893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552390714	chr6:167610941-167610942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs80302352	chr6:167610947-167610948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	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
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1835 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167609200-167609600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr6:167609400-167610600	Enhancers	Fetal Brain Male	brain
3	chr6:167609800-167610600	Active TSS	Placenta Amnion	Placenta Amnion
4	chr6:167610600-167611000	Enhancers	Placenta Amnion	Placenta Amnion
5	chr6:167610600-167615400	Weak transcription	Fetal Brain Male	brain
6	chr6:167610800-167612800	Weak transcription	Fetal Intestine Small	intestine
7	chr6:167611000-167613000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr6:167612800-167613000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:167612800-167615000	Strong transcription	Fetal Intestine Small	intestine
10	chr6:167613000-167613600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:167613000-167613800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:167613000-167616600	Enhancers	Placenta Amnion	Placenta Amnion
13	chr6:167613600-167613800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:167613800-167614400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:167613800-167622200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:167614000-167615400	Enhancers	HepG2	liver
17	chr6:167614200-167614400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr6:167614400-167614800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr6:167614400-167623200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr6:167614800-167616400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr6:167615000-167616800	Weak transcription	Fetal Intestine Small	intestine
22	chr6:167615400-167616400	Weak transcription	HepG2	liver
23	chr6:167615400-167617400	Enhancers	Fetal Brain Male	brain
24	chr6:167615800-167616200	Enhancers	Fetal Lung	lung
25	chr6:167615800-167628800	Weak transcription	Right Atrium	heart
26	chr6:167616400-167617000	Enhancers	HepG2	liver
27	chr6:167616400-167617400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr6:167616400-167617600	Enhancers	Rectal Smooth Muscle	rectum
29	chr6:167616600-167617200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr6:167616600-167617800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr6:167616600-167618400	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr6:167616800-167617200	Enhancers	Stomach Smooth Muscle	stomach
33	chr6:167616800-167617400	Bivalent Enhancer	K562	blood
34	chr6:167616800-167617600	Enhancers	Fetal Intestine Small	intestine
35	chr6:167617000-167617400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr6:167617000-167617400	Enhancers	Liver	Liver
37	chr6:167617000-167617400	Enhancers	Fetal Heart	heart
38	chr6:167617000-167617400	Enhancers	Fetal Intestine Large	intestine
39	chr6:167617000-167617400	Enhancers	Lung	lung
40	chr6:167617000-167617400	Active TSS	A549	lung
41	chr6:167617000-167617400	Flanking Active TSS	HepG2	liver
42	chr6:167617000-167617400	Enhancers	NH-A	brain
43	chr6:167617200-167617400	Enhancers	Colon Smooth Muscle	Colon
44	chr6:167617200-167617400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
45	chr6:167617400-167618200	Weak transcription	NH-A	brain
46	chr6:167617400-167618600	Weak transcription	Fetal Brain Male	brain
47	chr6:167617400-167619000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr6:167617400-167620800	Enhancers	HepG2	liver
49	chr6:167617400-167622400	Weak transcription	Fetal Intestine Large	intestine
50	chr6:167617600-167618000	Weak transcription	Fetal Intestine Small	intestine

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