Variant report

Variant	nsv1017088
Chromosome Location	chr6:167614471-167785109
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2705)
CpG islands
(count:4338)
Chromatin interactive
region (count:33)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2705 , 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	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167652605-167653007	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167651727-167651738	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167624462-167624811	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167633428-167633974	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:167682223-167682912	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:167645950-167646149	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:167637599-167638030	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:167655013-167655211	HepG2	liver:	n/a	n/a
13	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
14	ARID3A	chr6:167632046-167632420	HepG2	liver:	n/a	n/a
15	ARID3A	chr6:167628930-167629130	HepG2	liver:	n/a	n/a
16	ARID3A	chr6:167629887-167630151	HepG2	liver:	n/a	n/a
17	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
18	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
19	ARID3A	chr6:167629415-167629646	HepG2	liver:	n/a	n/a
20	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
21	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
22	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr6:167641333-167641936	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr6:167651500-167652487	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	chr6:167626020-167626431	GM12878	blood:	n/a	n/a
28	ATF2	chr6:167641353-167641826	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:167637370-167637829	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr6:167702257-167702472	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr6:167641591-167641850	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr6:167631950-167632087	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	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
36	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
37	BATF	chr6:167631870-167632155	GM12878	blood:	n/a	n/a
38	BATF	chr6:167625959-167626402	GM12878	blood:	n/a	n/a
39	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
40	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
41	BATF	chr6:167625794-167626502	GM12878	blood:	n/a	n/a
42	BATF	chr6:167702166-167702414	GM12878	blood:	n/a	n/a
43	BATF	chr6:167726053-167726251	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	chr6:167723198-167723690	HepG2	liver:	n/a	n/a
48	BHLHE40	chr6:167682232-167682824	HepG2	liver:	n/a	n/a
49	BHLHE40	chr6:167764869-167765070	K562	blood:	n/a	n/a
50	BHLHE40	chr6:167637543-167637955	HepG2	liver:	n/a	n/a

(count:4338 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167649384-167649434	HCM	heart:	n/a
2	chr6:167649384-167649434	AG04450	lung:	fetal
3	chr6:167703894-167703944	HUVEC	blood vessel:	n/a
4	chr6:167756099-167756149	HCM	heart:	n/a
5	chr6:167765110-167765160	HepG2	liver:	n/a
6	chr6:167658907-167658957	SK-N-SH	brain:	n/a
7	chr6:167704188-167704238	SK-N-SH	brain:	n/a
8	chr6:167649384-167649434	HCM	heart:	n/a
9	chr6:167649384-167649434	AG04450	lung:	fetal
10	chr6:167703894-167703944	HUVEC	blood vessel:	n/a
11	chr6:167756099-167756149	HCM	heart:	n/a
12	chr6:167765110-167765160	HepG2	liver:	n/a
13	chr6:167658907-167658957	SK-N-SH	brain:	n/a
14	chr6:167704188-167704238	SK-N-SH	brain:	n/a
15	chr6:167654977-167655027	H1-hESC	embryonic stem cell:	embryo
16	chr6:167633955-167634005	HCF	heart:	n/a
17	chr6:167763320-167763370	NHBE	bronchial:	n/a
18	chr6:167738592-167738642	Hela-S3	cervix:	n/a
19	chr6:167635072-167635122	SK-N-MC	brain:	n/a
20	chr6:167653907-167653957	AG09319	gingival:	n/a
21	chr6:167737937-167737987	HNPCEpiC	eye:	n/a
22	chr6:167655290-167655340	NT2-D1	testis:	n/a
23	chr6:167632873-167632923	K562	blood:	n/a
24	chr6:167649539-167649589	GM12892	blood:	n/a
25	chr6:167737937-167737987	HCPEpiC	choroid plexus:	n/a
26	chr6:167738425-167738475	T-47D	breast:	n/a
27	chr6:167709237-167709287	MCF10A-Er-Src	breast:	n/a
28	chr6:167710360-167710410	SKMC	muscle:	n/a
29	chr6:167761204-167761254	SK-N-MC	brain:	n/a
30	chr6:167703894-167703944	Hela-S3	cervix:	n/a
31	chr6:167655053-167655103	HRCEpiC	kidney:	n/a
32	chr6:167727700-167727750	BE2_C	brain:	n/a
33	chr6:167718461-167718511	IMR90	lung:	fetal
34	chr6:167622441-167622491	ProgFib	skin:	n/a
35	chr6:167633955-167634005	BE2_C	brain:	n/a
36	chr6:167704673-167704723	PANC-1	pancreas:	n/a
37	chr6:167616968-167617018	SK-N-MC	brain:	n/a
38	chr6:167765110-167765160	MCF-7	breast:	n/a
39	chr6:167661905-167661955	AG10803	skin:	n/a
40	chr6:167763819-167763869	Jurkat	blood:	n/a
41	chr6:167718461-167718511	HCM	heart:	n/a
42	chr6:167616968-167617018	HL-60	blood:	n/a
43	chr6:167637331-167637381	HCF	heart:	n/a
44	chr6:167635072-167635122	SAEC	small airway:	n/a
45	chr6:167654977-167655027	GM12891	blood:	n/a
46	chr6:167704808-167704858	HL-60	blood:	n/a
47	chr6:167631788-167631838	HUVEC	blood vessel:	n/a
48	chr6:167653982-167654032	HCPEpiC	choroid plexus:	n/a
49	chr6:167704769-167704819	A549	lung:	n/a
50	chr6:167653907-167653957	Hepatocyte	liver:	n/a

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

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

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

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

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
ENSG00000112494	chromatin interactions
ENSG00000216966	chromatin interactions
CYBASC3	miRNA target sites
CYB5R4	miRNA target sites

Extended variants
information (count: 8432 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:8432 , 50 per page) page: 1 2 3 4 5 6 7 ... 169

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143507718	chr6:167614481-167614482	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs535009388	chr6:167614495-167614496	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141930043	chr6:167614527-167614528	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553503067	chr6:167614530-167614531	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147293240	chr6:167614561-167614562	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542443252	chr6:167614581-167614582	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563417793	chr6:167614592-167614593	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140851167	chr6:167614624-167614625	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184231897	chr6:167614662-167614663	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564145472	chr6:167614681-167614682	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12665391	chr6:167614733-167614734	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs559488394	chr6:167614734-167614735	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188734216	chr6:167614782-167614783	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559636693	chr6:167614811-167614812	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541012985	chr6:167614845-167614846	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529828505	chr6:167614899-167614900	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs9457285	chr6:167614977-167614978	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs370358197	chr6:167615006-167615007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2180713	chr6:167615010-167615011	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs143098185	chr6:167615030-167615031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs9459913	chr6:167615057-167615058	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs147458457	chr6:167615135-167615136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs193187141	chr6:167615185-167615186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575102048	chr6:167615249-167615250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs9457286	chr6:167615299-167615300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs139233165	chr6:167615308-167615309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183328171	chr6:167615318-167615319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs112405106	chr6:167615406-167615407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575290948	chr6:167615415-167615416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545918014	chr6:167615427-167615428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs386708557	chr6:167615428-167615429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs145603541	chr6:167615439-167615440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573141212	chr6:167615441-167615442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540652394	chr6:167615442-167615443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376066311	chr6:167615446-167615447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs371797189	chr6:167615467-167615468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs148476739	chr6:167615473-167615474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563477570	chr6:167615474-167615475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs9459914	chr6:167615493-167615494	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs552317202	chr6:167615502-167615503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187411298	chr6:167615504-167615505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs9457287	chr6:167615508-167615509	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs546618719	chr6:167615528-167615529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144116697	chr6:167615572-167615573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535752521	chr6:167615606-167615607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557083154	chr6:167615611-167615612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569126555	chr6:167615612-167615613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567942367	chr6:167615679-167615680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539681593	chr6:167615716-167615717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191842869	chr6:167615732-167615733	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:1825 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167610600-167615400	Weak transcription	Fetal Brain Male	brain
2	chr6:167612800-167615000	Strong transcription	Fetal Intestine Small	intestine
3	chr6:167613000-167616600	Enhancers	Placenta Amnion	Placenta Amnion
4	chr6:167613800-167622200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:167614000-167615400	Enhancers	HepG2	liver
6	chr6:167614400-167614800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:167614400-167623200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr6:167614800-167616400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:167615000-167616800	Weak transcription	Fetal Intestine Small	intestine
10	chr6:167615400-167616400	Weak transcription	HepG2	liver
11	chr6:167615400-167617400	Enhancers	Fetal Brain Male	brain
12	chr6:167615800-167616200	Enhancers	Fetal Lung	lung
13	chr6:167615800-167628800	Weak transcription	Right Atrium	heart
14	chr6:167616400-167617000	Enhancers	HepG2	liver
15	chr6:167616400-167617400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr6:167616400-167617600	Enhancers	Rectal Smooth Muscle	rectum
17	chr6:167616600-167617200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr6:167616600-167617800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr6:167616600-167618400	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr6:167616800-167617200	Enhancers	Stomach Smooth Muscle	stomach
21	chr6:167616800-167617400	Bivalent Enhancer	K562	blood
22	chr6:167616800-167617600	Enhancers	Fetal Intestine Small	intestine
23	chr6:167617000-167617400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr6:167617000-167617400	Enhancers	Liver	Liver
25	chr6:167617000-167617400	Enhancers	Fetal Heart	heart
26	chr6:167617000-167617400	Enhancers	Fetal Intestine Large	intestine
27	chr6:167617000-167617400	Enhancers	Lung	lung
28	chr6:167617000-167617400	Active TSS	A549	lung
29	chr6:167617000-167617400	Flanking Active TSS	HepG2	liver
30	chr6:167617000-167617400	Enhancers	NH-A	brain
31	chr6:167617200-167617400	Enhancers	Colon Smooth Muscle	Colon
32	chr6:167617200-167617400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
33	chr6:167617400-167618200	Weak transcription	NH-A	brain
34	chr6:167617400-167618600	Weak transcription	Fetal Brain Male	brain
35	chr6:167617400-167619000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr6:167617400-167620800	Enhancers	HepG2	liver
37	chr6:167617400-167622400	Weak transcription	Fetal Intestine Large	intestine
38	chr6:167617600-167618000	Weak transcription	Fetal Intestine Small	intestine
39	chr6:167617600-167618000	Weak transcription	Rectal Smooth Muscle	rectum
40	chr6:167617600-167618200	Weak transcription	Colon Smooth Muscle	Colon
41	chr6:167618000-167619000	Enhancers	Fetal Intestine Small	intestine
42	chr6:167618000-167619000	Enhancers	Rectal Smooth Muscle	rectum
43	chr6:167618200-167618400	Enhancers	Colon Smooth Muscle	Colon
44	chr6:167618400-167618600	Enhancers	NH-A	brain
45	chr6:167618400-167619000	Enhancers	Placenta Amnion	Placenta Amnion
46	chr6:167618400-167624400	Weak transcription	Colon Smooth Muscle	Colon
47	chr6:167618600-167619200	Enhancers	Fetal Brain Male	brain
48	chr6:167619000-167619200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr6:167619000-167620200	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr6:167619000-167622400	Weak transcription	Fetal Intestine Small	intestine

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