Variant report

Variant	nsv1019761
Chromosome Location	chr6:167597233-167652883
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:977)
CpG islands
(count:1159)
Chromatin interactive
region (count:8)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167652605-167653007	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167633428-167633974	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167624462-167624811	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167637599-167638030	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167632046-167632420	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167629415-167629646	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167645950-167646149	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167629887-167630151	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:167628930-167629130	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:167651727-167651738	HepG2	liver:	n/a	n/a
11	ATF2	chr6:167626020-167626431	GM12878	blood:	n/a	n/a
12	ATF2	chr6:167625939-167626508	GM12878	blood:	n/a	n/a
13	ATF2	chr6:167651500-167652487	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr6:167641333-167641936	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr6:167641353-167641826	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr6:167637370-167637829	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:167641591-167641850	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:167631950-167632087	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr6:167631870-167632155	GM12878	blood:	n/a	n/a
20	BATF	chr6:167625959-167626402	GM12878	blood:	n/a	n/a
21	BATF	chr6:167625794-167626502	GM12878	blood:	n/a	n/a
22	BCL11A	chr6:167626130-167626424	GM12878	blood:	n/a	n/a
23	BHLHE40	chr6:167617544-167617803	K562	blood:	n/a	n/a
24	BHLHE40	chr6:167617588-167617796	HepG2	liver:	n/a	n/a
25	BHLHE40	chr6:167631891-167632258	HepG2	liver:	n/a	n/a
26	BHLHE40	chr6:167631930-167632149	K562	blood:	n/a	n/a
27	BHLHE40	chr6:167626013-167626185	GM12878	blood:	n/a	n/a
28	BHLHE40	chr6:167631978-167632147	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:167637543-167637955	HepG2	liver:	n/a	n/a
30	BHLHE40	chr6:167629939-167630334	HepG2	liver:	n/a	n/a
31	BHLHE40	chr6:167617441-167617909	HepG2	liver:	n/a	n/a
32	BHLHE40	chr6:167629860-167630298	HepG2	liver:	n/a	n/a
33	BHLHE40	chr6:167617148-167617887	HepG2	liver:	n/a	n/a
34	BRCA1	chr6:167633650-167633694	HepG2	liver:	n/a	n/a
35	BRCA1	chr6:167625284-167625312	HepG2	liver:	n/a	n/a
36	BRCA1	chr6:167624418-167624607	HepG2	liver:	n/a	n/a
37	CBX3	chr6:167637348-167638006	HCT-116	colon:	n/a	n/a
38	CBX3	chr6:167617380-167617754	K562	blood:	n/a	n/a
39	CEBPB	chr6:167629950-167630124	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:167629863-167630222	HepG2	liver:	n/a	n/a
41	CEBPB	chr6:167603633-167603660	K562	blood:	n/a	n/a
42	CEBPB	chr6:167639701-167639901	K562	blood:	n/a	chr6:167639837-167639848 chr6:167639839-167639848 chr6:167639839-167639850
43	CEBPB	chr6:167639685-167640004	H1-hESC	embryonic stem cell:	n/a	chr6:167639837-167639848 chr6:167639839-167639848 chr6:167639839-167639850
44	CEBPB	chr6:167639673-167640002	HepG2	liver:	n/a	chr6:167639837-167639848 chr6:167639839-167639848 chr6:167639839-167639850
45	CEBPB	chr6:167624471-167624762	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:167652443-167653271	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:167629456-167629648	HepG2	liver:	n/a	chr6:167629574-167629585 chr6:167629574-167629585 chr6:167629572-167629585
48	CEBPB	chr6:167633762-167634102	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:167629904-167630160	HepG2	liver:	n/a	n/a
50	CEBPB	chr6:167629908-167630318	HepG2	liver:	n/a	n/a

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167631788-167631838	PANC-1	pancreas:	n/a
2	chr6:167652028-167652078	RPTEC	kidney:	n/a
3	chr6:167649631-167649681	HNPCEpiC	eye:	n/a
4	chr6:167652028-167652078	NHDF-neo	bronchial:	n/a
5	chr6:167649384-167649434	K562	blood:	n/a
6	chr6:167622441-167622491	ovcar-3	ovarian:	n/a
7	chr6:167617119-167617169	MCF-7	breast:	n/a
8	chr6:167633022-167633072	PrEC	prostate:	n/a
9	chr6:167633955-167634005	AG04449	skin:	fetal
10	chr6:167635072-167635122	U87	brain:	n/a
11	chr6:167632873-167632923	HCT-116	colon:	n/a
12	chr6:167637331-167637381	ECC-1	luminal epithelium:	n/a
13	chr6:167652028-167652078	SK-N-SH_RA	brain:	n/a
14	chr6:167649539-167649589	A549	lung:	n/a
15	chr6:167637331-167637381	HepG2	liver:	n/a
16	chr6:167652028-167652078	HCPEpiC	choroid plexus:	n/a
17	chr6:167637331-167637381	HCT-116	colon:	n/a
18	chr6:167633022-167633072	HMEC	breast:	n/a
19	chr6:167652028-167652078	ECC-1	luminal epithelium:	n/a
20	chr6:167637331-167637381	HUVEC	blood vessel:	n/a
21	chr6:167649749-167649799	NHDF-neo	bronchial:	n/a
22	chr6:167622441-167622491	HCT-116	colon:	n/a
23	chr6:167617119-167617169	HEK293	kidney:	embryo
24	chr6:167652028-167652078	Hela-S3	cervix:	n/a
25	chr6:167649256-167649306	K562	blood:	n/a
26	chr6:167632873-167632923	AoSMC	blood vessel:	n/a
27	chr6:167649336-167649386	SK-N-MC	brain:	n/a
28	chr6:167649631-167649681	BE2_C	brain:	n/a
29	chr6:167634139-167634189	HEK293	kidney:	embryo
30	chr6:167622441-167622491	HAEpiC	amniotic membrane:	n/a
31	chr6:167649539-167649589	LNCaP	prostate:	n/a
32	chr6:167649384-167649434	GM12878	blood:	n/a
33	chr6:167649631-167649681	NHDF-neo	bronchial:	n/a
34	chr6:167635072-167635122	Hepatocyte	liver:	n/a
35	chr6:167649749-167649799	HMEC	breast:	n/a
36	chr6:167652028-167652078	HCM	heart:	n/a
37	chr6:167633022-167633072	AG09319	gingival:	n/a
38	chr6:167632873-167632923	GM12878	blood:	n/a
39	chr6:167649384-167649434	T-47D	breast:	n/a
40	chr6:167649539-167649589	HRE	kidney:	n/a
41	chr6:167632873-167632923	BJ	skin:	n/a
42	chr6:167631788-167631838	SK-N-SH	brain:	n/a
43	chr6:167633022-167633072	GM06990	blood:	n/a
44	chr6:167623149-167623199	NHBE	bronchial:	n/a
45	chr6:167622441-167622491	AG09319	gingival:	n/a
46	chr6:167622441-167622491	PFSK-1	brain:	n/a
47	chr6:167635072-167635122	PANC-1	pancreas:	n/a
48	chr6:167649631-167649681	NB4	blood:	n/a
49	chr6:167649384-167649434	PrEC	prostate:	n/a
50	chr6:167635072-167635122	MCF-7	breast:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167623945..167626187-chr6:168297648..168300373,2	K562	blood:
2	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
3	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
4	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
5	chr6:167620399..167623068-chr6:167623897..167626646,2	K562	blood:
6	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
7	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
8	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR31-1	chr6:167651156-167651293	XLOC_005921
2	lnc-GPR31-1	chr6:167650996-167651293	XLOC_005921

No data

Variant related genes	Relation type
TCP10L2	TF binding region
ENSG00000228648	TF binding region
ENSG00000216966	TF binding region
TCP10L2	CpG island
ENSG00000228648	CpG island
ENSG00000216966	CpG island
ENSG00000216966	chromatin interactions
CYB5R4	miRNA target sites

Extended variants
information (count: 2409 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2409 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544532847	chr6:167597235-167597236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551151519	chr6:167597244-167597245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183904148	chr6:167597259-167597260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545145282	chr6:167597269-167597270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560643322	chr6:167597287-167597288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527822361	chr6:167597326-167597327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543004125	chr6:167597333-167597334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201482426	chr6:167597348-167597349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189045792	chr6:167597358-167597359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529184430	chr6:167597368-167597369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569737022	chr6:167597375-167597376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs62439194	chr6:167597406-167597407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12201674	chr6:167597426-167597427	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs192984094	chr6:167597427-167597428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551151353	chr6:167597444-167597445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552211223	chr6:167597463-167597464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566553933	chr6:167597467-167597468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7771648	chr6:167597527-167597528	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs4710195	chr6:167597532-167597533	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs566958180	chr6:167597533-167597534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551748753	chr6:167597546-167597547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556462650	chr6:167597547-167597548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9366099	chr6:167597549-167597550	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs144709561	chr6:167597566-167597567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577923660	chr6:167597570-167597571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539032426	chr6:167597573-167597574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554116222	chr6:167597582-167597583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs71554324	chr6:167597615-167597616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113855587	chr6:167597621-167597622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572481696	chr6:167597629-167597630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370093771	chr6:167597631-167597632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7772924	chr6:167597638-167597639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112408955	chr6:167597650-167597651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7758329	chr6:167597669-167597670	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs531757376	chr6:167597680-167597681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544469173	chr6:167597686-167597687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575805249	chr6:167597709-167597710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs7762372	chr6:167597727-167597728	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs533118946	chr6:167597734-167597735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551552363	chr6:167597751-167597752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566581763	chr6:167597752-167597753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527364870	chr6:167597753-167597754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548820658	chr6:167597754-167597755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566896111	chr6:167597756-167597757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537452325	chr6:167597764-167597765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs60899859	chr6:167597779-167597780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555779113	chr6:167597781-167597782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs397755322	chr6:167597789-167597790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571602729	chr6:167597806-167597807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538991850	chr6:167597808-167597809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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

Chromatin state (count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167597200-167598200	Weak transcription	HepG2	liver
2	chr6:167598200-167598400	Enhancers	HepG2	liver
3	chr6:167609200-167609600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:167609400-167610600	Enhancers	Fetal Brain Male	brain
5	chr6:167609800-167610600	Active TSS	Placenta Amnion	Placenta Amnion
6	chr6:167610600-167611000	Enhancers	Placenta Amnion	Placenta Amnion
7	chr6:167610600-167615400	Weak transcription	Fetal Brain Male	brain
8	chr6:167610800-167612800	Weak transcription	Fetal Intestine Small	intestine
9	chr6:167611000-167613000	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr6:167612800-167613000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:167612800-167615000	Strong transcription	Fetal Intestine Small	intestine
12	chr6:167613000-167613600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:167613000-167613800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr6:167613000-167616600	Enhancers	Placenta Amnion	Placenta Amnion
15	chr6:167613600-167613800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:167613800-167614400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:167613800-167622200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:167614000-167615400	Enhancers	HepG2	liver
19	chr6:167614200-167614400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr6:167614400-167614800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr6:167614400-167623200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr6:167614800-167616400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr6:167615000-167616800	Weak transcription	Fetal Intestine Small	intestine
24	chr6:167615400-167616400	Weak transcription	HepG2	liver
25	chr6:167615400-167617400	Enhancers	Fetal Brain Male	brain
26	chr6:167615800-167616200	Enhancers	Fetal Lung	lung
27	chr6:167615800-167628800	Weak transcription	Right Atrium	heart
28	chr6:167616400-167617000	Enhancers	HepG2	liver
29	chr6:167616400-167617400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr6:167616400-167617600	Enhancers	Rectal Smooth Muscle	rectum
31	chr6:167616600-167617200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr6:167616600-167617800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr6:167616600-167618400	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr6:167616800-167617200	Enhancers	Stomach Smooth Muscle	stomach
35	chr6:167616800-167617400	Bivalent Enhancer	K562	blood
36	chr6:167616800-167617600	Enhancers	Fetal Intestine Small	intestine
37	chr6:167617000-167617400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr6:167617000-167617400	Enhancers	Liver	Liver
39	chr6:167617000-167617400	Enhancers	Fetal Heart	heart
40	chr6:167617000-167617400	Enhancers	Fetal Intestine Large	intestine
41	chr6:167617000-167617400	Enhancers	Lung	lung
42	chr6:167617000-167617400	Active TSS	A549	lung
43	chr6:167617000-167617400	Flanking Active TSS	HepG2	liver
44	chr6:167617000-167617400	Enhancers	NH-A	brain
45	chr6:167617200-167617400	Enhancers	Colon Smooth Muscle	Colon
46	chr6:167617200-167617400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
47	chr6:167617400-167618200	Weak transcription	NH-A	brain
48	chr6:167617400-167618600	Weak transcription	Fetal Brain Male	brain
49	chr6:167617400-167619000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr6:167617400-167620800	Enhancers	HepG2	liver

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