Variant report

Variant	nsv482516
Chromosome Location	chr6:167672161-167845924
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2180)
CpG islands
(count:5070)
Chromatin interactive
region (count:28)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2180 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167682223-167682912	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167834911-167835243	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:167837621-167838022	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:167811767-167812223	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:167809998-167810531	HepG2	liver:	n/a	n/a
13	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
14	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
15	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:167702257-167702472	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr6:167785311-167785621	GM12878	blood:	n/a	n/a
21	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
22	BATF	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
23	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
24	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
25	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
26	BATF	chr6:167801477-167801674	GM12878	blood:	n/a	n/a
27	BATF	chr6:167702166-167702414	GM12878	blood:	n/a	n/a
28	BCL11A	chr6:167801472-167801775	GM12878	blood:	n/a	n/a
29	BCL11A	chr6:167801474-167801790	GM12878	blood:	n/a	n/a
30	BCL11A	chr6:167800632-167800815	GM12878	blood:	n/a	n/a
31	BCL11A	chr6:167799353-167799569	GM12878	blood:	n/a	n/a
32	BCL11A	chr6:167801917-167802109	GM12878	blood:	n/a	n/a
33	BCL11A	chr6:167836935-167837429	GM12878	blood:	n/a	n/a
34	BCL3	chr6:167710341-167710705	GM12878	blood:	n/a	n/a
35	BCLAF1	chr6:167764829-167765189	GM12878	blood:	n/a	chr6:167764879-167764888 chr6:167765036-167765044
36	BHLHE40	chr6:167764869-167765070	K562	blood:	n/a	n/a
37	BHLHE40	chr6:167704696-167705644	HepG2	liver:	n/a	n/a
38	BHLHE40	chr6:167691769-167691891	K562	blood:	n/a	chr6:167691854-167691867
39	BHLHE40	chr6:167834738-167835231	HepG2	liver:	n/a	n/a
40	BHLHE40	chr6:167814832-167815507	HepG2	liver:	n/a	chr6:167815146-167815155 chr6:167815144-167815157 chr6:167815147-167815156 chr6:167815140-167815161 chr6:167815146-167815155
41	BHLHE40	chr6:167722070-167722725	HepG2	liver:	n/a	chr6:167722523-167722539
42	BHLHE40	chr6:167702264-167702463	HepG2	liver:	n/a	n/a
43	BHLHE40	chr6:167811642-167812135	HepG2	liver:	n/a	n/a
44	BHLHE40	chr6:167723198-167723690	HepG2	liver:	n/a	n/a
45	BHLHE40	chr6:167732490-167732554	GM12878	blood:	n/a	n/a
46	BHLHE40	chr6:167699851-167700081	HepG2	liver:	n/a	n/a
47	BHLHE40	chr6:167702270-167702451	K562	blood:	n/a	n/a
48	BHLHE40	chr6:167810045-167810579	HepG2	liver:	n/a	n/a
49	BHLHE40	chr6:167785339-167785655	HepG2	liver:	n/a	n/a
50	BHLHE40	chr6:167764785-167765457	GM12878	blood:	n/a	n/a

(count:5070 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167709720-167709770	HEK293	kidney:	embryo
2	chr6:167738342-167738392	HUVEC	blood vessel:	n/a
3	chr6:167789195-167789245	HL-60	blood:	n/a
4	chr6:167789441-167789491	CMK	blood:	n/a
5	chr6:167791024-167791074	HMEC	breast:	n/a
6	chr6:167709720-167709770	HRCEpiC	kidney:	n/a
7	chr6:167789195-167789245	HCF	heart:	n/a
8	chr6:167709720-167709770	HEK293	kidney:	embryo
9	chr6:167738342-167738392	HUVEC	blood vessel:	n/a
10	chr6:167789195-167789245	HL-60	blood:	n/a
11	chr6:167789441-167789491	CMK	blood:	n/a
12	chr6:167791024-167791074	HMEC	breast:	n/a
13	chr6:167709720-167709770	HRCEpiC	kidney:	n/a
14	chr6:167789195-167789245	HCF	heart:	n/a
15	chr6:167705750-167705800	IMR90	lung:	fetal
16	chr6:167792181-167792231	HMEC	breast:	n/a
17	chr6:167704673-167704723	GM19239	blood:	n/a
18	chr6:167808551-167808601	HCM	heart:	n/a
19	chr6:167717313-167717363	T-47D	breast:	n/a
20	chr6:167792181-167792231	PANC-1	pancreas:	n/a
21	chr6:167717196-167717246	BJ	skin:	n/a
22	chr6:167704808-167704858	CMK	blood:	n/a
23	chr6:167792181-167792231	T-47D	breast:	n/a
24	chr6:167786059-167786109	IMR90	lung:	fetal
25	chr6:167703894-167703944	IMR90	lung:	fetal
26	chr6:167695026-167695076	PFSK-1	brain:	n/a
27	chr6:167835969-167836019	GM19239	blood:	n/a
28	chr6:167717196-167717246	SK-N-SH_RA	brain:	n/a
29	chr6:167680447-167680497	NB4	blood:	n/a
30	chr6:167810395-167810445	NB4	blood:	n/a
31	chr6:167839518-167839568	HPAEpiC	pulmonary alveolar:	n/a
32	chr6:167704808-167704858	U87	brain:	n/a
33	chr6:167738594-167738644	NB4	blood:	n/a
34	chr6:167738594-167738644	GM12891	blood:	n/a
35	chr6:167762783-167762833	AG09319	gingival:	n/a
36	chr6:167717313-167717363	GM12891	blood:	n/a
37	chr6:167704769-167704819	AG10803	skin:	n/a
38	chr6:167704188-167704238	HCM	heart:	n/a
39	chr6:167816104-167816154	HepG2	liver:	n/a
40	chr6:167794374-167794424	MCF10A-Er-Src	breast:	n/a
41	chr6:167717196-167717246	HCF	heart:	n/a
42	chr6:167810343-167810393	HCF	heart:	n/a
43	chr6:167764620-167764670	SAEC	small airway:	n/a
44	chr6:167809972-167810022	NH-A	brain:	n/a
45	chr6:167704188-167704238	GM06990	blood:	n/a
46	chr6:167791114-167791164	GM19239	blood:	n/a
47	chr6:167810343-167810393	SK-N-SH_RA	brain:	n/a
48	chr6:167738594-167738644	NHDF-neo	bronchial:	n/a
49	chr6:167704808-167704858	HL-60	blood:	n/a
50	chr6:167810343-167810393	HAEpiC	amniotic membrane:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167813417..167815135-chr6:167817698..167819518,2	K562	blood:
2	chr6:167703616..167705764-chr6:167717598..167719278,2	MCF-7	breast:
3	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
4	chr6:167823826..167826272-chr6:167829672..167831832,2	K562	blood:
5	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
6	chr6:167818746..167821496-chr6:167831177..167833070,2	K562	blood:
7	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
8	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
9	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
10	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
11	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
12	chr20:57615578..57617834-chr6:167831422..167833295,2	MCF-7	breast:
13	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
14	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
15	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
16	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
17	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
18	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
19	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
20	chr6:167818746..167821496-chr6:167831177..167833070,2	K562	blood:
21	chr6:167823826..167826272-chr6:167829672..167831832,2	K562	blood:
22	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
23	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
24	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
25	chr6:167699179..167702166-chr6:167703091..167705361,2	K562	blood:
26	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
27	chr6:167813417..167815135-chr6:167817698..167819518,2	K562	blood:
28	chr1:28836187..28837925-chr6:167694572..167696254,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCP10-3	chr6:167826637-167827774	ucscGeneNc_uc003qvy_1
2	lnc-TTLL2-2	chr6:167840757-167840858	NONHSAT116104
3	lnc-TCP10-3	chr6:167823155-167825466	ucscGeneNc_uc003qvy_1
4	lnc-TCP10-3	chr6:167825862-167825976	ucscGeneNc_uc003qvy_1
5	lnc-TTLL2-1	chr6:167804760-167804979	XLOC_005541
6	lnc-TCP10-2	chr6:167810373-167814438	ucscGeneNc_uc003qvx_1
7	lnc-TCP10-2	chr6:167822441-167822752	ucscGeneNc_uc003qvx_1
8	lnc-TCP10-3	chr6:167838864-167838906	ucscGeneNc_uc003qvy_1
9	lnc-TTLL2-2	chr6:167837702-167837948	NONHSAT116104
10	lnc-TTLL2-1	chr6:167803650-167803969	XLOC_005541
11	lnc-TCP10-2	chr6:167821589-167821728	ucscGeneNc_uc003qvx_1
12	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094
13	lnc-TCP10-1	chr6:167787839-167789289	NONHSAT116097
14	lnc-TCP10-1	chr6:167786578-167786848	NONHSAT116097
15	lnc-TCP10-3	chr6:167839445-167839616	ucscGeneNc_uc003qvy_1
16	lnc-TCP10-3	chr6:167839733-167839819	ucscGeneNc_uc003qvy_1
17	lnc-UNC93A-3	chr6:167764293-167764966	NONHSAT116095
18	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095

No data

Variant related genes	Relation type
UNC93A	TF binding region
TCP10	TF binding region
TTLL2	TF binding region
ENSG00000217447	TF binding region
UNC93A	CpG island
TCP10	CpG island
TTLL2	CpG island
ENSG00000217447	CpG island
ENSG00000112494	chromatin interactions
ENSG00000180198	chromatin interactions
ENSG00000101166	chromatin interactions

Extended variants
information (count: 8101 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:8101 , 50 per page) page: 1 2 3 4 5 6 7 ... 163

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140883130	chr6:167672214-167672215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542683356	chr6:167672219-167672220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs80248042	chr6:167672220-167672221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574022605	chr6:167672231-167672232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs544414574	chr6:167672246-167672247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562673254	chr6:167672249-167672250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150141962	chr6:167672256-167672257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551472677	chr6:167672259-167672260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs56210545	chr6:167672272-167672273	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs376081221	chr6:167672321-167672322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs57044478	chr6:167672329-167672330	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs182818473	chr6:167672330-167672331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187115771	chr6:167672378-167672379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538193942	chr6:167672398-167672399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138565559	chr6:167672409-167672410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs149275513	chr6:167672435-167672436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577174751	chr6:167672437-167672438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115674032	chr6:167672462-167672463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557208682	chr6:167672463-167672464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536639699	chr6:167672465-167672466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs6923713	chr6:167672466-167672467	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs573932706	chr6:167672472-167672473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371111943	chr6:167672512-167672513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544530141	chr6:167672521-167672522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147371551	chr6:167672533-167672534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191547885	chr6:167672544-167672545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs59311096	chr6:167672556-167672557	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs143458992	chr6:167672593-167672594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2183707	chr6:167672610-167672611	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs542212472	chr6:167672616-167672617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372028724	chr6:167672625-167672626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531844790	chr6:167672643-167672644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2346159	chr6:167672725-167672726	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs531850641	chr6:167672743-167672744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147138989	chr6:167672753-167672754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571873007	chr6:167672754-167672755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs77171637	chr6:167672756-167672757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1854858	chr6:167672883-167672884	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs184574573	chr6:167672886-167672887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs187490674	chr6:167672943-167672944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1854859	chr6:167672992-167672993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
42	rs113872175	chr6:167673021-167673022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1854860	chr6:167673030-167673031	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs139342539	chr6:167673031-167673032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538112712	chr6:167673068-167673069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556402928	chr6:167673075-167673076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371471029	chr6:167673183-167673184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577896806	chr6:167673236-167673237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545180560	chr6:167673280-167673281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs79161817	chr6:167673289-167673290	Weak transcription	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1428 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167669200-167673000	Enhancers	HepG2	liver
2	chr6:167671600-167672200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:167672200-167672600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:167672600-167672800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:167672800-167680200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:167673000-167674000	Weak transcription	HepG2	liver
7	chr6:167674000-167675000	Enhancers	HepG2	liver
8	chr6:167675000-167678600	Weak transcription	HepG2	liver
9	chr6:167678400-167679600	Enhancers	Fetal Intestine Large	intestine
10	chr6:167678400-167682400	Enhancers	Fetal Intestine Small	intestine
11	chr6:167678600-167679800	Enhancers	HepG2	liver
12	chr6:167678800-167679000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr6:167678800-167679400	Enhancers	Fetal Kidney	kidney
14	chr6:167678800-167679800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:167679000-167679600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr6:167679000-167679800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:167679000-167683200	Enhancers	Duodenum Mucosa	Duodenum
18	chr6:167679200-167679400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr6:167679200-167679400	Enhancers	Stomach Mucosa	stomach
20	chr6:167679400-167679800	Enhancers	Fetal Muscle Leg	muscle
21	chr6:167679400-167680200	Weak transcription	Fetal Kidney	kidney
22	chr6:167679400-167680400	Weak transcription	Stomach Mucosa	stomach
23	chr6:167679600-167680400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr6:167679600-167680400	Weak transcription	Fetal Intestine Large	intestine
25	chr6:167679800-167680200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr6:167679800-167680200	Weak transcription	Fetal Muscle Leg	muscle
27	chr6:167679800-167680200	Weak transcription	HepG2	liver
28	chr6:167679800-167680400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:167680000-167680200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr6:167680000-167680200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
31	chr6:167680000-167680200	Active TSS	Stomach Smooth Muscle	stomach
32	chr6:167680200-167680400	Flanking Active TSS	Stomach Smooth Muscle	stomach
33	chr6:167680200-167680800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr6:167680200-167681000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr6:167680200-167681000	Enhancers	Fetal Kidney	kidney
36	chr6:167680200-167681000	Enhancers	Fetal Muscle Leg	muscle
37	chr6:167680200-167682000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:167680200-167682400	Enhancers	HepG2	liver
39	chr6:167680400-167680600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:167680400-167680600	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr6:167680400-167680800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:167680400-167681000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr6:167680400-167681800	Enhancers	Esophagus	oesophagus
44	chr6:167680400-167682000	Enhancers	Fetal Thymus	thymus
45	chr6:167680400-167682400	Enhancers	Fetal Intestine Large	intestine
46	chr6:167680400-167682600	Enhancers	Stomach Mucosa	stomach
47	chr6:167680600-167680800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr6:167680600-167681000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:167680600-167681200	Enhancers	Gastric	stomach
50	chr6:167680600-167681400	Weak transcription	Sigmoid Colon	Sigmoid Colon

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