Variant report

Variant	nsv886944
Chromosome Location	chr6:167604257-167724650
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2085)
CpG islands
(count:2812)
Chromatin interactive
region (count:22)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2085 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167632046-167632420	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167651727-167651738	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167629887-167630151	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167633428-167633974	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167629415-167629646	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:167682223-167682912	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:167645950-167646149	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:167628930-167629130	HepG2	liver:	n/a	n/a
13	ARID3A	chr6:167624462-167624811	HepG2	liver:	n/a	n/a
14	ARID3A	chr6:167655013-167655211	HepG2	liver:	n/a	n/a
15	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
16	ARID3A	chr6:167637599-167638030	HepG2	liver:	n/a	n/a
17	ARID3A	chr6:167652605-167653007	HepG2	liver:	n/a	n/a
18	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
19	ATF2	chr6:167641353-167641826	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr6:167625939-167626508	GM12878	blood:	n/a	n/a
21	ATF2	chr6:167651500-167652487	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr6:167641333-167641936	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr6:167626020-167626431	GM12878	blood:	n/a	n/a
24	BACH1	chr6:167637370-167637829	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr6:167702257-167702472	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr6:167641591-167641850	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr6:167631950-167632087	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr6:167625794-167626502	GM12878	blood:	n/a	n/a
29	BATF	chr6:167625959-167626402	GM12878	blood:	n/a	n/a
30	BATF	chr6:167631870-167632155	GM12878	blood:	n/a	n/a
31	BATF	chr6:167702166-167702414	GM12878	blood:	n/a	n/a
32	BCL11A	chr6:167626130-167626424	GM12878	blood:	n/a	n/a
33	BCL3	chr6:167710341-167710705	GM12878	blood:	n/a	n/a
34	BHLHE40	chr6:167723177-167724281	HepG2	liver:	n/a	n/a
35	BHLHE40	chr6:167702264-167702463	HepG2	liver:	n/a	n/a
36	BHLHE40	chr6:167629939-167630334	HepG2	liver:	n/a	n/a
37	BHLHE40	chr6:167631891-167632258	HepG2	liver:	n/a	n/a
38	BHLHE40	chr6:167617588-167617796	HepG2	liver:	n/a	n/a
39	BHLHE40	chr6:167617148-167617887	HepG2	liver:	n/a	n/a
40	BHLHE40	chr6:167637543-167637955	HepG2	liver:	n/a	n/a
41	BHLHE40	chr6:167631978-167632147	GM12878	blood:	n/a	n/a
42	BHLHE40	chr6:167699851-167700081	HepG2	liver:	n/a	n/a
43	BHLHE40	chr6:167702270-167702451	K562	blood:	n/a	n/a
44	BHLHE40	chr6:167631930-167632149	K562	blood:	n/a	n/a
45	BHLHE40	chr6:167722070-167722725	HepG2	liver:	n/a	chr6:167722523-167722539
46	BHLHE40	chr6:167617441-167617909	HepG2	liver:	n/a	n/a
47	BHLHE40	chr6:167682232-167682824	HepG2	liver:	n/a	n/a
48	BHLHE40	chr6:167626013-167626185	GM12878	blood:	n/a	n/a
49	BHLHE40	chr6:167629860-167630298	HepG2	liver:	n/a	n/a
50	BHLHE40	chr6:167617544-167617803	K562	blood:	n/a	n/a

(count:2812 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167653957-167654007	H1-hESC	embryonic stem cell:	embryo
2	chr6:167633955-167634005	HMEC	breast:	n/a
3	chr6:167655053-167655103	HepG2	liver:	n/a
4	chr6:167653982-167654032	A549	lung:	n/a
5	chr6:167622202-167622252	SK-N-SH_RA	brain:	n/a
6	chr6:167680447-167680497	GM12891	blood:	n/a
7	chr6:167653957-167654007	H1-hESC	embryonic stem cell:	embryo
8	chr6:167633955-167634005	HMEC	breast:	n/a
9	chr6:167655053-167655103	HepG2	liver:	n/a
10	chr6:167653982-167654032	A549	lung:	n/a
11	chr6:167622202-167622252	SK-N-SH_RA	brain:	n/a
12	chr6:167680447-167680497	GM12891	blood:	n/a
13	chr6:167717196-167717246	GM12891	blood:	n/a
14	chr6:167704188-167704238	HRPEpiC	eye:	n/a
15	chr6:167704673-167704723	RPTEC	kidney:	n/a
16	chr6:167703591-167703641	T-47D	breast:	n/a
17	chr6:167617119-167617169	MCF10A-Er-Src	breast:	n/a
18	chr6:167649256-167649306	PANC-1	pancreas:	n/a
19	chr6:167704769-167704819	ovcar-3	ovarian:	n/a
20	chr6:167617119-167617169	Hela-S3	cervix:	n/a
21	chr6:167708827-167708877	LNCaP	prostate:	n/a
22	chr6:167649631-167649681	HCPEpiC	choroid plexus:	n/a
23	chr6:167622202-167622252	H1-hESC	embryonic stem cell:	embryo
24	chr6:167703894-167703944	IMR90	lung:	fetal
25	chr6:167652028-167652078	PrEC	prostate:	n/a
26	chr6:167680455-167680505	Jurkat	blood:	n/a
27	chr6:167703591-167703641	Caco-2	colon:	n/a
28	chr6:167617119-167617169	H1-hESC	embryonic stem cell:	embryo
29	chr6:167703894-167703944	NB4	blood:	n/a
30	chr6:167704673-167704723	Hepatocyte	liver:	n/a
31	chr6:167704808-167704858	HCT-116	colon:	n/a
32	chr6:167655053-167655103	GM12878	blood:	n/a
33	chr6:167649539-167649589	LNCaP	prostate:	n/a
34	chr6:167704673-167704723	HEEpiC	esophagus:	n/a
35	chr6:167634139-167634189	HIPEpiC	eye:	n/a
36	chr6:167655290-167655340	HNPCEpiC	eye:	n/a
37	chr6:167680447-167680497	AG04449	skin:	fetal
38	chr6:167617119-167617169	GM06990	blood:	n/a
39	chr6:167703591-167703641	GM06990	blood:	n/a
40	chr6:167649539-167649589	AG09319	gingival:	n/a
41	chr6:167655053-167655103	HCT-116	colon:	n/a
42	chr6:167680447-167680497	AG10803	skin:	n/a
43	chr6:167649539-167649589	HCF	heart:	n/a
44	chr6:167649749-167649799	HIPEpiC	eye:	n/a
45	chr6:167718461-167718511	T-47D	breast:	n/a
46	chr6:167653982-167654032	GM12891	blood:	n/a
47	chr6:167658907-167658957	AG04449	skin:	fetal
48	chr6:167623149-167623199	NHDF-neo	bronchial:	n/a
49	chr6:167700000-167700050	CMK	blood:	n/a
50	chr6:167653982-167654032	CMK	blood:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
2	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
3	chr6:167620399..167623068-chr6:167623897..167626646,2	K562	blood:
4	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
5	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
6	chr6:167668192..167671777-chr6:167684157..167687082,3	K562	blood:
7	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
8	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
9	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
10	chr6:167623945..167626187-chr6:168297648..168300373,2	K562	blood:
11	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
12	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
13	chr6:167699179..167702166-chr6:167703091..167705361,2	K562	blood:
14	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
15	chr6:167703616..167705764-chr6:167717598..167719278,2	MCF-7	breast:
16	chr6:167669951..167671777-chr6:167683631..167687000,3	K562	blood:
17	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
18	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
19	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
20	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
21	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
22	chr1:28836187..28837925-chr6:167694572..167696254,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC93A-1	chr6:167659275-167659404	XLOC_005540
2	lnc-GPR31-1	chr6:167653636-167653833	XLOC_005921
3	lnc-UNC93A-1	chr6:167655379-167655453	XLOC_005540
4	lnc-GPR31-1	chr6:167650996-167651293	XLOC_005921
5	lnc-GPR31-1	chr6:167653688-167653968	XLOC_005921
6	lnc-GPR31-1	chr6:167651156-167651293	XLOC_005921

No data

Variant related genes	Relation type
UNC93A	TF binding region
ENSG00000228648	TF binding region
ENSG00000231720	TF binding region
ENSG00000216966	TF binding region
TCP10L2	TF binding region
UNC93A	CpG island
ENSG00000228648	CpG island
ENSG00000231720	CpG island
ENSG00000216966	CpG island
TCP10L2	CpG island
ENSG00000216966	chromatin interactions
ENSG00000112494	chromatin interactions
ENSG00000180198	chromatin interactions
CYB5R4	miRNA target sites
CYBASC3	miRNA target sites

Extended variants
information (count: 6042 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:6042 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552664749	chr6:167604456-167604457	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs570711010	chr6:167604472-167604473	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs536172859	chr6:167604593-167604594	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs35601830	chr6:167604598-167604599	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs371168704	chr6:167604658-167604659	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs566938718	chr6:167604666-167604667	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs188079933	chr6:167604667-167604668	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs149211981	chr6:167604707-167604708	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs191521496	chr6:167604739-167604740	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs576906306	chr6:167604756-167604757	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs115524879	chr6:167604758-167604759	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs552598450	chr6:167604763-167604764	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs113316349	chr6:167604768-167604769	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs575170516	chr6:167604844-167604845	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs542558212	chr6:167604866-167604867	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs570858029	chr6:167604867-167604868	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs369198472	chr6:167604868-167604869	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs145666618	chr6:167604891-167604892	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs528306810	chr6:167606275-167606276	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs546860322	chr6:167606292-167606293	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs59635969	chr6:167606310-167606311	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs535228591	chr6:167606312-167606313	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs2345972	chr6:167606343-167606344	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs556878999	chr6:167606344-167606345	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs564544023	chr6:167606415-167606416	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs568779896	chr6:167606456-167606457	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs372062240	chr6:167606490-167606491	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs549810512	chr6:167609205-167609206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532249362	chr6:167609206-167609207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs187038722	chr6:167609221-167609222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs9364894	chr6:167609268-167609269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536441242	chr6:167609270-167609271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9348230	chr6:167609271-167609272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569716314	chr6:167609277-167609278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs9366103	chr6:167609283-167609284	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs576909957	chr6:167609284-167609285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs9348231	chr6:167609301-167609302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9347181	chr6:167609302-167609303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575078034	chr6:167609330-167609331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542388385	chr6:167609388-167609389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs142868866	chr6:167609427-167609428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2860557	chr6:167609435-167609436	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs191425925	chr6:167609453-167609454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183293475	chr6:167609461-167609462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs199812756	chr6:167609464-167609465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs111298897	chr6:167609465-167609466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs67196505	chr6:167609490-167609491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs409115	chr6:167609492-167609493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548330853	chr6:167609493-167609494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs420718	chr6:167609500-167609501	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:1194 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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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