Variant report

Variant	nsv1030424
Chromosome Location	chr6:167685635-167774950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1376)
CpG islands
(count:2567)
Chromatin interactive
region (count:20)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1376 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
8	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
9	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
10	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr6:167702257-167702472	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
16	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
17	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
18	BATF	chr6:167702166-167702414	GM12878	blood:	n/a	n/a
19	BATF	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
20	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
21	BCL3	chr6:167710341-167710705	GM12878	blood:	n/a	n/a
22	BCLAF1	chr6:167764829-167765189	GM12878	blood:	n/a	chr6:167764879-167764888 chr6:167765036-167765044
23	BHLHE40	chr6:167722146-167722527	HepG2	liver:	n/a	n/a
24	BHLHE40	chr6:167723177-167724281	HepG2	liver:	n/a	n/a
25	BHLHE40	chr6:167691769-167691891	K562	blood:	n/a	chr6:167691854-167691867
26	BHLHE40	chr6:167704696-167705644	HepG2	liver:	n/a	n/a
27	BHLHE40	chr6:167723198-167723690	HepG2	liver:	n/a	n/a
28	BHLHE40	chr6:167699851-167700081	HepG2	liver:	n/a	n/a
29	BHLHE40	chr6:167733252-167733970	HepG2	liver:	n/a	n/a
30	BHLHE40	chr6:167702264-167702463	HepG2	liver:	n/a	n/a
31	BHLHE40	chr6:167733370-167733629	HepG2	liver:	n/a	n/a
32	BHLHE40	chr6:167702270-167702451	K562	blood:	n/a	n/a
33	BHLHE40	chr6:167764869-167765070	K562	blood:	n/a	n/a
34	BHLHE40	chr6:167754879-167756141	HepG2	liver:	n/a	n/a
35	BHLHE40	chr6:167722070-167722725	HepG2	liver:	n/a	chr6:167722523-167722539
36	BHLHE40	chr6:167732490-167732554	GM12878	blood:	n/a	n/a
37	BHLHE40	chr6:167755635-167755964	HepG2	liver:	n/a	n/a
38	BHLHE40	chr6:167755531-167755951	HepG2	liver:	n/a	n/a
39	BHLHE40	chr6:167764785-167765457	GM12878	blood:	n/a	n/a
40	BRCA1	chr6:167764922-167765205	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr6:167722055-167722521	HepG2	liver:	n/a	n/a
42	BRCA1	chr6:167750805-167750846	HepG2	liver:	n/a	n/a
43	CBX3	chr6:167702109-167702642	K562	blood:	n/a	n/a
44	CBX3	chr6:167708857-167709379	K562	blood:	n/a	n/a
45	CBX3	chr6:167708762-167709384	K562	blood:	n/a	n/a
46	CEBPB	chr6:167764886-167765190	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr6:167705138-167705428	K562	blood:	n/a	chr6:167705263-167705276 chr6:167705265-167705274 chr6:167705263-167705274
48	CEBPB	chr6:167762489-167763000	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:167693321-167693632	H1-hESC	embryonic stem cell:	n/a	chr6:167693472-167693481 chr6:167693471-167693482 chr6:167693470-167693481 chr6:167693601-167693614
50	CEBPB	chr6:167715387-167715550	HepG2	liver:	n/a	chr6:167715514-167715525 chr6:167715513-167715526

(count:2567 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167704769-167704819	SAEC	small airway:	n/a
2	chr6:167763819-167763869	SK-N-SH_RA	brain:	n/a
3	chr6:167738277-167738327	HepG2	liver:	n/a
4	chr6:167762783-167762833	GM06990	blood:	n/a
5	chr6:167704188-167704238	HRE	kidney:	n/a
6	chr6:167704769-167704819	SAEC	small airway:	n/a
7	chr6:167763819-167763869	SK-N-SH_RA	brain:	n/a
8	chr6:167738277-167738327	HepG2	liver:	n/a
9	chr6:167762783-167762833	GM06990	blood:	n/a
10	chr6:167704188-167704238	HRE	kidney:	n/a
11	chr6:167738342-167738392	SAEC	small airway:	n/a
12	chr6:167738425-167738475	K562	blood:	n/a
13	chr6:167756099-167756149	CMK	blood:	n/a
14	chr6:167738592-167738642	AoSMC	blood vessel:	n/a
15	chr6:167738425-167738475	HIPEpiC	eye:	n/a
16	chr6:167762783-167762833	HIPEpiC	eye:	n/a
17	chr6:167753807-167753857	GM06990	blood:	n/a
18	chr6:167709720-167709770	HCF	heart:	n/a
19	chr6:167709720-167709770	NH-A	brain:	n/a
20	chr6:167764967-167765017	ProgFib	skin:	n/a
21	chr6:167738277-167738327	GM19239	blood:	n/a
22	chr6:167703894-167703944	SAEC	small airway:	n/a
23	chr6:167734054-167734104	HIPEpiC	eye:	n/a
24	chr6:167704673-167704723	SK-N-SH_RA	brain:	n/a
25	chr6:167705253-167705303	SK-N-SH	brain:	n/a
26	chr6:167763819-167763869	PrEC	prostate:	n/a
27	chr6:167763320-167763370	HCPEpiC	choroid plexus:	n/a
28	chr6:167765215-167765265	ProgFib	skin:	n/a
29	chr6:167738277-167738327	T-47D	breast:	n/a
30	chr6:167738425-167738475	GM06990	blood:	n/a
31	chr6:167738594-167738644	H1-hESC	embryonic stem cell:	embryo
32	chr6:167738277-167738327	GM12878	blood:	n/a
33	chr6:167703894-167703944	BJ	skin:	n/a
34	chr6:167753807-167753857	GM12878	blood:	n/a
35	chr6:167705253-167705303	NB4	blood:	n/a
36	chr6:167761204-167761254	GM12891	blood:	n/a
37	chr6:167704808-167704858	PFSK-1	brain:	n/a
38	chr6:167765215-167765265	AoSMC	blood vessel:	n/a
39	chr6:167762783-167762833	GM12878	blood:	n/a
40	chr6:167710360-167710410	Caco-2	colon:	n/a
41	chr6:167764146-167764196	Hela-S3	cervix:	n/a
42	chr6:167762783-167762833	HCM	heart:	n/a
43	chr6:167703591-167703641	Caco-2	colon:	n/a
44	chr6:167737937-167737987	K562	blood:	n/a
45	chr6:167709720-167709770	MCF-7	breast:	n/a
46	chr6:167753807-167753857	A549	lung:	n/a
47	chr6:167753807-167753857	HepG2	liver:	n/a
48	chr6:167718461-167718511	ECC-1	luminal epithelium:	n/a
49	chr6:167695026-167695076	NHBE	bronchial:	n/a
50	chr6:167704188-167704238	RPTEC	kidney:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167699179..167702166-chr6:167703091..167705361,2	K562	blood:
2	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
3	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
4	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
5	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
6	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
7	chr1:28836187..28837925-chr6:167694572..167696254,2	K562	blood:
8	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
9	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
10	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
11	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
12	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
13	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
14	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
15	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
16	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
17	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
18	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
19	chr6:167703616..167705764-chr6:167717598..167719278,2	MCF-7	breast:
20	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095
2	lnc-UNC93A-3	chr6:167764293-167764966	NONHSAT116095
3	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094

No data

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

Extended variants
information (count: 4299 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4299 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2092090	chr6:167685635-167685636	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs145471860	chr6:167685654-167685655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564206664	chr6:167685664-167685665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115825913	chr6:167685672-167685673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2092091	chr6:167685688-167685689	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs73255082	chr6:167685723-167685724	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs529573551	chr6:167685766-167685767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561033405	chr6:167685779-167685780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373147398	chr6:167685796-167685797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185437101	chr6:167685816-167685817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569085757	chr6:167685830-167685831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs539677251	chr6:167685843-167685844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557820636	chr6:167685844-167685845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566668991	chr6:167685863-167685864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534149835	chr6:167685895-167685896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs451841	chr6:167685911-167685912	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs148410155	chr6:167685915-167685916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189854905	chr6:167685926-167685927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557322524	chr6:167685954-167685955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112736813	chr6:167685991-167685992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs151126607	chr6:167686006-167686007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546062900	chr6:167686008-167686009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141094987	chr6:167686025-167686026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78115217	chr6:167686030-167686031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77440152	chr6:167686031-167686032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540187483	chr6:167686040-167686041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs561549401	chr6:167686041-167686042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs146767738	chr6:167686051-167686052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192021931	chr6:167686082-167686083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562883669	chr6:167686096-167686097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs147918823	chr6:167686133-167686134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551561662	chr6:167686195-167686196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183904435	chr6:167686207-167686208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534050057	chr6:167686232-167686233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188395971	chr6:167686266-167686267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567531918	chr6:167686300-167686301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141664848	chr6:167686304-167686305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147055578	chr6:167686319-167686320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs191795064	chr6:167686331-167686332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs13191136	chr6:167686340-167686341	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs368989129	chr6:167686387-167686388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182794530	chr6:167686406-167686407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs117956574	chr6:167686419-167686420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539925771	chr6:167686420-167686421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561853669	chr6:167686423-167686424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138202473	chr6:167686459-167686460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187073673	chr6:167686461-167686462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191675488	chr6:167686470-167686471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533455123	chr6:167686471-167686472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551524848	chr6:167686473-167686474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1021 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167681800-167689000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:167682800-167688000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:167682800-167688400	Enhancers	Fetal Intestine Large	intestine
4	chr6:167682800-167688600	Enhancers	Fetal Intestine Small	intestine
5	chr6:167683000-167688000	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr6:167683000-167688800	Enhancers	HepG2	liver
7	chr6:167683000-167690200	Weak transcription	Liver	Liver
8	chr6:167683600-167687000	Enhancers	Duodenum Mucosa	Duodenum
9	chr6:167684200-167687000	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr6:167684800-167687000	Enhancers	Stomach Mucosa	stomach
11	chr6:167685000-167686600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr6:167685000-167691800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr6:167685200-167685800	Enhancers	Fetal Heart	heart
14	chr6:167685600-167685800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr6:167685600-167685800	Enhancers	Gastric	stomach
16	chr6:167685600-167686600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:167685600-167688000	Weak transcription	Esophagus	oesophagus
18	chr6:167685800-167686600	Weak transcription	Gastric	stomach
19	chr6:167685800-167691600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr6:167686000-167686800	Weak transcription	Small Intestine	intestine
21	chr6:167686600-167687000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr6:167686600-167687000	Enhancers	Gastric	stomach
23	chr6:167686600-167687200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr6:167687000-167688600	Weak transcription	Gastric	stomach
25	chr6:167687000-167690400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr6:167688000-167689200	Enhancers	Placenta Amnion	Placenta Amnion
27	chr6:167688000-167689400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr6:167688000-167689400	Enhancers	Esophagus	oesophagus
29	chr6:167688000-167691600	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr6:167688200-167688400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr6:167688400-167689200	Enhancers	Lung	lung
32	chr6:167688400-167690000	Weak transcription	Fetal Intestine Large	intestine
33	chr6:167688600-167689000	Enhancers	Gastric	stomach
34	chr6:167688600-167692600	Weak transcription	Fetal Intestine Small	intestine
35	chr6:167688800-167689400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr6:167688800-167689400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr6:167688800-167690200	Weak transcription	HepG2	liver
38	chr6:167689000-167689200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr6:167689000-167694800	Weak transcription	Gastric	stomach
40	chr6:167689200-167702400	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr6:167689400-167690400	Weak transcription	Esophagus	oesophagus
42	chr6:167689400-167690600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr6:167690000-167690600	Enhancers	Fetal Intestine Large	intestine
44	chr6:167690200-167690400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr6:167690200-167691400	Enhancers	Liver	Liver
46	chr6:167690200-167691600	Enhancers	HepG2	liver
47	chr6:167690400-167690600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr6:167690400-167690600	ZNF genes & repeats	Esophagus	oesophagus
49	chr6:167690600-167690800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
50	chr6:167690600-167690800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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