Variant report

Variant	nsv886948
Chromosome Location	chr6:167783664-167832036
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167809998-167810531	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167811767-167812223	HepG2	liver:	n/a	n/a
3	BATF	chr6:167801477-167801674	GM12878	blood:	n/a	n/a
4	BATF	chr6:167785311-167785621	GM12878	blood:	n/a	n/a
5	BCL11A	chr6:167801917-167802109	GM12878	blood:	n/a	n/a
6	BCL11A	chr6:167801472-167801775	GM12878	blood:	n/a	n/a
7	BCL11A	chr6:167801474-167801790	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:167799353-167799569	GM12878	blood:	n/a	n/a
9	BCL11A	chr6:167800632-167800815	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:167815066-167815240	K562	blood:	n/a	chr6:167815146-167815155 chr6:167815144-167815157 chr6:167815147-167815156 chr6:167815140-167815161 chr6:167815146-167815155
11	BHLHE40	chr6:167785339-167785655	HepG2	liver:	n/a	n/a
12	BHLHE40	chr6:167810045-167810579	HepG2	liver:	n/a	n/a
13	BHLHE40	chr6:167811642-167812135	HepG2	liver:	n/a	n/a
14	BHLHE40	chr6:167826030-167826420	HepG2	liver:	n/a	n/a
15	BHLHE40	chr6:167811648-167812302	HepG2	liver:	n/a	n/a
16	BHLHE40	chr6:167814832-167815507	HepG2	liver:	n/a	chr6:167815146-167815155 chr6:167815144-167815157 chr6:167815147-167815156 chr6:167815140-167815161 chr6:167815146-167815155
17	BHLHE40	chr6:167827209-167827450	K562	blood:	n/a	n/a
18	BRCA1	chr6:167811846-167812095	HepG2	liver:	n/a	n/a
19	CBX3	chr6:167800537-167800803	K562	blood:	n/a	n/a
20	CEBPB	chr6:167810129-167810428	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:167823739-167824431	HepG2	liver:	n/a	chr6:167824329-167824338 chr6:167824327-167824340
22	CEBPB	chr6:167811682-167811930	HepG2	liver:	n/a	n/a
23	CEBPB	chr6:167811663-167812136	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:167830864-167831090	HepG2	liver:	n/a	chr6:167831007-167831018
25	CHD1	chr6:167807154-167807163	GM12878	blood:	n/a	n/a
26	CHD2	chr6:167812114-167812170	HepG2	liver:	n/a	n/a
27	CHD2	chr6:167811596-167811760	HepG2	liver:	n/a	n/a
28	CHD2	chr6:167815273-167815334	HepG2	liver:	n/a	n/a
29	CTCF	chr6:167789460-167789610	HEK293	kidney:	n/a	n/a
30	CTCF	chr6:167785355-167785612	MCF-7	breast:	n/a	chr6:167785486-167785494 chr6:167785474-167785495 chr6:167785481-167785494 chr6:167785480-167785496 chr6:167785479-167785497 chr6:167785481-167785494
31	CTCF	chr6:167785185-167785694	K562	blood:	n/a	chr6:167785486-167785494 chr6:167785474-167785495 chr6:167785481-167785494 chr6:167785480-167785496 chr6:167785479-167785497 chr6:167785481-167785494
32	CTCF	chr6:167785358-167785628	Lung_OC	lung:	n/a	chr6:167785486-167785494 chr6:167785474-167785495 chr6:167785481-167785494 chr6:167785480-167785496 chr6:167785479-167785497 chr6:167785481-167785494
33	CTCF	chr6:167806024-167806089	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr6:167821134-167821274	HepG2	liver:	n/a	n/a
35	CTCF	chr6:167815000-167815150	HEK293	kidney:	n/a	n/a
36	CTCF	chr6:167785250-167785676	K562	blood:	n/a	chr6:167785486-167785494 chr6:167785474-167785495 chr6:167785481-167785494 chr6:167785480-167785496 chr6:167785479-167785497 chr6:167785481-167785494
37	CTCF	chr6:167785335-167785614	GM19240	blood:	n/a	chr6:167785486-167785494 chr6:167785474-167785495 chr6:167785481-167785494 chr6:167785480-167785496 chr6:167785479-167785497 chr6:167785481-167785494
38	CTCF	chr6:167785319-167785633	LNCaP	prostate:	n/a	chr6:167785486-167785494 chr6:167785474-167785495 chr6:167785481-167785494 chr6:167785480-167785496 chr6:167785479-167785497 chr6:167785481-167785494
39	CTCF	chr6:167783740-167783765	K562	blood:	n/a	n/a
40	CTCF	chr6:167786760-167786910	GM12872	blood:	n/a	n/a
41	CTCF	chr6:167785339-167785617	MCF-7	breast:	n/a	chr6:167785486-167785494 chr6:167785474-167785495 chr6:167785481-167785494 chr6:167785480-167785496 chr6:167785479-167785497 chr6:167785481-167785494
42	CTCF	chr6:167785347-167785617	GM10248	blood:	n/a	chr6:167785486-167785494 chr6:167785474-167785495 chr6:167785481-167785494 chr6:167785480-167785496 chr6:167785479-167785497 chr6:167785481-167785494
43	CTCF	chr6:167785333-167785616	GM19238	blood:	n/a	chr6:167785486-167785494 chr6:167785474-167785495 chr6:167785481-167785494 chr6:167785480-167785496 chr6:167785479-167785497 chr6:167785481-167785494
44	CTCF	chr6:167785620-167785770	AG09319	gingival:	n/a	n/a
45	CTCF	chr6:167815360-167815510	HEK293	kidney:	n/a	n/a
46	CTCF	chr6:167785453-167785628	K562	blood:	n/a	chr6:167785486-167785494 chr6:167785474-167785495 chr6:167785481-167785494 chr6:167785480-167785496 chr6:167785479-167785497 chr6:167785481-167785494
47	CTCF	chr6:167789420-167789570	HEK293	kidney:	n/a	n/a
48	CTCF	chr6:167785355-167785608	ProgFib	skin:	n/a	chr6:167785486-167785494 chr6:167785474-167785495 chr6:167785481-167785494 chr6:167785480-167785496 chr6:167785479-167785497 chr6:167785481-167785494
49	CTCF	chr6:167789400-167789550	Caco-2	colon:	n/a	n/a
50	CTCF	chr6:167784907-167784952	LNCaP	prostate:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167786592-167786642	AoSMC	blood vessel:	n/a
2	chr6:167810343-167810393	Jurkat	blood:	n/a
3	chr6:167791153-167791203	HEK293	kidney:	embryo
4	chr6:167786592-167786642	AoSMC	blood vessel:	n/a
5	chr6:167810343-167810393	Jurkat	blood:	n/a
6	chr6:167791153-167791203	HEK293	kidney:	embryo
7	chr6:167814257-167814307	H1-hESC	embryonic stem cell:	embryo
8	chr6:167794374-167794424	HepG2	liver:	n/a
9	chr6:167792741-167792791	A549	lung:	n/a
10	chr6:167814397-167814447	H1-hESC	embryonic stem cell:	embryo
11	chr6:167814257-167814307	AG04450	lung:	fetal
12	chr6:167810343-167810393	H1-hESC	embryonic stem cell:	embryo
13	chr6:167794374-167794424	SKMC	muscle:	n/a
14	chr6:167792181-167792231	MCF-7	breast:	n/a
15	chr6:167810043-167810093	SK-N-SH	brain:	n/a
16	chr6:167791114-167791164	SK-N-SH_RA	brain:	n/a
17	chr6:167808366-167808416	PrEC	prostate:	n/a
18	chr6:167809876-167809926	IMR90	lung:	fetal
19	chr6:167786059-167786109	AG10803	skin:	n/a
20	chr6:167810343-167810393	SK-N-MC	brain:	n/a
21	chr6:167808366-167808416	MCF10A-Er-Src	breast:	n/a
22	chr6:167814257-167814307	SK-N-SH_RA	brain:	n/a
23	chr6:167789539-167789589	SK-N-SH	brain:	n/a
24	chr6:167791153-167791203	HCT-116	colon:	n/a
25	chr6:167809825-167809875	ECC-1	luminal epithelium:	n/a
26	chr6:167789441-167789491	HCF	heart:	n/a
27	chr6:167789539-167789589	HRE	kidney:	n/a
28	chr6:167791153-167791203	NB4	blood:	n/a
29	chr6:167791153-167791203	HIPEpiC	eye:	n/a
30	chr6:167786642-167786692	HEEpiC	esophagus:	n/a
31	chr6:167814397-167814447	HNPCEpiC	eye:	n/a
32	chr6:167791153-167791203	AoSMC	blood vessel:	n/a
33	chr6:167794506-167794556	HEK293	kidney:	embryo
34	chr6:167810043-167810093	MCF-7	breast:	n/a
35	chr6:167814314-167814364	SK-N-MC	brain:	n/a
36	chr6:167794506-167794556	GM12878	blood:	n/a
37	chr6:167786059-167786109	AoSMC	blood vessel:	n/a
38	chr6:167791114-167791164	GM12892	blood:	n/a
39	chr6:167809876-167809926	MCF-7	breast:	n/a
40	chr6:167808366-167808416	PANC-1	pancreas:	n/a
41	chr6:167797877-167797927	BE2_C	brain:	n/a
42	chr6:167792741-167792791	NHDF-neo	bronchial:	n/a
43	chr6:167786642-167786692	HCT-116	colon:	n/a
44	chr6:167791153-167791203	HNPCEpiC	eye:	n/a
45	chr6:167808551-167808601	AoSMC	blood vessel:	n/a
46	chr6:167810043-167810093	Jurkat	blood:	n/a
47	chr6:167814257-167814307	Hela-S3	cervix:	n/a
48	chr6:167791114-167791164	K562	blood:	n/a
49	chr6:167814257-167814307	AG10803	skin:	n/a
50	chr6:167809876-167809926	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:167823826..167826272-chr6:167829672..167831832,2	K562	blood:
2	chr6:167818746..167821496-chr6:167831177..167833070,2	K562	blood:
3	chr6:167823826..167826272-chr6:167829672..167831832,2	K562	blood:
4	chr6:167813417..167815135-chr6:167817698..167819518,2	K562	blood:
5	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
6	chr6:167813417..167815135-chr6:167817698..167819518,2	K562	blood:
7	chr20:57615578..57617834-chr6:167831422..167833295,2	MCF-7	breast:
8	chr6:167818746..167821496-chr6:167831177..167833070,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTLL2-1	chr6:167804760-167804979	XLOC_005541
2	lnc-TCP10-3	chr6:167825862-167825976	ucscGeneNc_uc003qvy_1
3	lnc-TCP10-3	chr6:167823155-167825466	ucscGeneNc_uc003qvy_1
4	lnc-TCP10-2	chr6:167810373-167814438	ucscGeneNc_uc003qvx_1
5	lnc-TCP10-1	chr6:167787839-167789289	NONHSAT116097
6	lnc-TCP10-2	chr6:167822441-167822752	ucscGeneNc_uc003qvx_1
7	lnc-TCP10-2	chr6:167821589-167821728	ucscGeneNc_uc003qvx_1
8	lnc-TTLL2-1	chr6:167803650-167803969	XLOC_005541
9	lnc-TCP10-3	chr6:167826637-167827774	ucscGeneNc_uc003qvy_1
10	lnc-TCP10-1	chr6:167786578-167786848	NONHSAT116097

Variant related genes	Relation type
TCP10	TF binding region
TCP10	CpG island
ENSG00000101166	chromatin interactions

Extended variants
information (count: 2059 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2059 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1831591	chr6:167783664-167783665	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537608835	chr6:167783668-167783669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1412440	chr6:167783676-167783677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555944483	chr6:167783678-167783679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577638233	chr6:167783683-167783684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192095545	chr6:167783690-167783691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555930263	chr6:167783694-167783695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553475650	chr6:167783717-167783718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369711794	chr6:167783718-167783719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572038040	chr6:167783720-167783721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543343169	chr6:167783722-167783723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561605945	chr6:167783727-167783728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184030880	chr6:167783736-167783737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543985470	chr6:167783737-167783738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373250119	chr6:167783748-167783749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187475204	chr6:167783750-167783751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200716543	chr6:167783790-167783791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547902975	chr6:167783807-167783808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192024489	chr6:167783839-167783840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530154828	chr6:167783870-167783871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535343843	chr6:167783886-167783887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548188343	chr6:167783895-167783896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs3124652	chr6:167784033-167784034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553685903	chr6:167784036-167784037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs3124653	chr6:167784047-167784048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs115599862	chr6:167784049-167784050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs9346740	chr6:167784054-167784055	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs146529993	chr6:167784066-167784067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571455953	chr6:167784074-167784075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545483768	chr6:167784080-167784081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557792803	chr6:167784090-167784091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142180020	chr6:167784095-167784096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553882354	chr6:167784112-167784113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs9364918	chr6:167784124-167784125	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs536211428	chr6:167784130-167784131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370223142	chr6:167784159-167784160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543586875	chr6:167784213-167784214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576780318	chr6:167784216-167784217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151200681	chr6:167784238-167784239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12530043	chr6:167784239-167784240	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs577396007	chr6:167784242-167784243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541709231	chr6:167784264-167784265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559758882	chr6:167784287-167784288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530137508	chr6:167784293-167784294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs117246249	chr6:167784303-167784304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541793959	chr6:167784323-167784324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563358682	chr6:167784329-167784330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531488215	chr6:167784330-167784331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549694114	chr6:167784341-167784342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs137958330	chr6:167784350-167784351	Weak transcription	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
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:165 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167777000-167784800	Weak transcription	HepG2	liver
2	chr6:167784800-167785400	Enhancers	HepG2	liver
3	chr6:167785000-167785400	Enhancers	Fetal Intestine Small	intestine
4	chr6:167785400-167786600	Weak transcription	Fetal Intestine Small	intestine
5	chr6:167785400-167786600	Weak transcription	HepG2	liver
6	chr6:167785800-167786200	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr6:167786200-167786600	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr6:167786400-167786600	Enhancers	Fetal Intestine Large	intestine
9	chr6:167786400-167786600	Enhancers	Rectal Mucosa Donor 29	rectum
10	chr6:167786600-167787000	Enhancers	Liver	Liver
11	chr6:167786600-167787000	Enhancers	Duodenum Mucosa	Duodenum
12	chr6:167786600-167787000	Flanking Active TSS	Fetal Intestine Large	intestine
13	chr6:167786600-167787000	Flanking Active TSS	Fetal Intestine Small	intestine
14	chr6:167786600-167787000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
15	chr6:167786600-167787000	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr6:167786600-167787000	Enhancers	Stomach Mucosa	stomach
17	chr6:167786600-167787000	Flanking Active TSS	HepG2	liver
18	chr6:167786800-167787000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
19	chr6:167787000-167787400	Enhancers	Fetal Intestine Large	intestine
20	chr6:167787000-167787600	Enhancers	HepG2	liver
21	chr6:167787000-167788000	Enhancers	Fetal Intestine Small	intestine
22	chr6:167787600-167791200	Weak transcription	HepG2	liver
23	chr6:167791000-167791200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
24	chr6:167791200-167791400	Enhancers	HepG2	liver
25	chr6:167791400-167791600	Bivalent Enhancer	HepG2	liver
26	chr6:167796200-167796400	Bivalent Enhancer	HepG2	liver
27	chr6:167807200-167807400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:167807200-167807600	Enhancers	Rectal Smooth Muscle	rectum
29	chr6:167807400-167807600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr6:167807400-167809600	Bivalent Enhancer	HepG2	liver
31	chr6:167807600-167814400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr6:167808200-167808400	Enhancers	Fetal Lung	lung
33	chr6:167808400-167809000	Weak transcription	Fetal Lung	lung
34	chr6:167809000-167809800	Enhancers	Fetal Lung	lung
35	chr6:167809200-167812600	Enhancers	Liver	Liver
36	chr6:167809200-167812800	Enhancers	Fetal Intestine Small	intestine
37	chr6:167809400-167811800	Enhancers	Stomach Mucosa	stomach
38	chr6:167809400-167812800	Enhancers	Fetal Intestine Large	intestine
39	chr6:167809600-167810400	Flanking Bivalent TSS/Enh	HepG2	liver
40	chr6:167809800-167810400	Weak transcription	Fetal Lung	lung
41	chr6:167809800-167810400	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr6:167810000-167810600	Enhancers	Pancreas	Pancrea
43	chr6:167810000-167811400	Enhancers	Gastric	stomach
44	chr6:167810400-167810600	Enhancers	Fetal Lung	lung
45	chr6:167810400-167810800	Flanking Active TSS	HepG2	liver
46	chr6:167810400-167811800	Enhancers	Spleen	Spleen
47	chr6:167810400-167814800	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr6:167810600-167811800	Weak transcription	Pancreas	Pancrea
49	chr6:167810800-167811600	Enhancers	HepG2	liver
50	chr6:167811000-167811800	Weak transcription	Lung	lung

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