Variant report

Variant	nsv1029530
Chromosome Location	chr6:166977678-167016052
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:607)
CpG islands
(count:610)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:607 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:167001393-167001971	GM12878	blood:	n/a	n/a
2	ATF2	chr6:167002299-167002766	GM12878	blood:	n/a	n/a
3	ATF3	chr6:167000270-167000513	K562	blood:	n/a	n/a
4	ATF3	chr6:167000246-167000648	GM12878	blood:	n/a	n/a
5	BACH1	chr6:166986298-166986452	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:166984538-166984622	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr6:167002902-167003124	GM12878	blood:	n/a	n/a
8	BATF	chr6:167002365-167002681	GM12878	blood:	n/a	chr6:167002529-167002540 chr6:167002530-167002540
9	BATF	chr6:167002317-167002739	GM12878	blood:	n/a	chr6:167002529-167002540 chr6:167002530-167002540
10	BCLAF1	chr6:167001220-167001927	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:166982668-166982947	K562	blood:	n/a	chr6:166982816-166982825 chr6:166982815-166982824 chr6:166982814-166982827 chr6:166982810-166982831 chr6:166982816-166982825
12	BHLHE40	chr6:167001637-167001815	GM12878	blood:	n/a	n/a
13	BRCA1	chr6:167002400-167002501	GM12878	blood:	n/a	n/a
14	CEBPB	chr6:166994353-166994587	IMR90	lung:	n/a	n/a
15	CEBPB	chr6:166987131-166987232	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr6:166981883-166982162	H1-hESC	embryonic stem cell:	n/a	chr6:166982056-166982067
17	CEBPB	chr6:167011583-167012430	IMR90	lung:	n/a	chr6:167011904-167011915 chr6:167011904-167011915 chr6:167011988-167011999
18	CEBPB	chr6:166981986-166982136	MCF-7	breast:	n/a	chr6:166982056-166982067
19	CEBPB	chr6:166996726-166996928	K562	blood:	n/a	n/a
20	CEBPB	chr6:167006322-167006709	IMR90	lung:	n/a	n/a
21	CEBPB	chr6:166985741-166986323	IMR90	lung:	n/a	n/a
22	CEBPB	chr6:166981890-166982250	K562	blood:	n/a	chr6:166982056-166982067
23	CEBPB	chr6:166981880-166982137	HepG2	liver:	n/a	chr6:166982056-166982067
24	CEBPB	chr6:166980420-166980981	IMR90	lung:	n/a	chr6:166980822-166980834
25	CEBPB	chr6:166981891-166982106	IMR90	lung:	n/a	chr6:166982056-166982067
26	CEBPB	chr6:167008545-167009247	IMR90	lung:	n/a	chr6:167008889-167008902
27	CHD1	chr6:167001325-167001722	GM12878	blood:	n/a	n/a
28	CHD1	chr6:167001924-167002124	GM12878	blood:	n/a	n/a
29	CHD2	chr6:167000269-167000599	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr6:167002930-167003130	GM12878	blood:	n/a	n/a
31	CHD2	chr6:167000293-167000620	K562	blood:	n/a	n/a
32	CHD2	chr6:167002275-167002388	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr6:167000282-167000605	GM12878	blood:	n/a	n/a
34	CHD2	chr6:167002247-167002564	GM12878	blood:	n/a	chr6:167002440-167002450
35	CHD2	chr6:166986159-166986511	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr6:167000296-167000639	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTBP2	chr6:166985986-166986826	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr6:167002220-167002370	GM12873	blood:	n/a	n/a
39	CTCF	chr6:166990179-166990235	GM13976	blood:	n/a	n/a
40	CTCF	chr6:167002900-167003050	AG04449	skin:	n/a	n/a
41	CTCF	chr6:166985960-166986110	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr6:167002700-167002850	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr6:166986320-166986470	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr6:166999814-166999877	GM10266	blood:	n/a	n/a
45	CTCF	chr6:167002825-167003092	GM12878	blood:	n/a	n/a
46	CTCF	chr6:166986340-166986490	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr6:167009580-167009730	AG04449	skin:	n/a	n/a
48	CTCF	chr6:167002820-167002970	HRE	kidney:	n/a	n/a
49	CTCF	chr6:167002880-167003030	GM12865	blood:	n/a	n/a
50	CTCF	chr6:166988820-166988970	AG10803	skin:	n/a	chr6:166988873-166988886

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:166993541-166993591	PANC-1	pancreas:	n/a
2	chr6:166984691-166984741	U87	brain:	n/a
3	chr6:166984607-166984657	AG09319	gingival:	n/a
4	chr6:166980629-166980679	ovcar-3	ovarian:	n/a
5	chr6:166986562-166986612	HEEpiC	esophagus:	n/a
6	chr6:166984691-166984741	NT2-D1	testis:	n/a
7	chr6:166986562-166986612	AG04450	lung:	fetal
8	chr6:166993541-166993591	PFSK-1	brain:	n/a
9	chr6:167002977-167003027	A549	lung:	n/a
10	chr6:167011311-167011361	GM19239	blood:	n/a
11	chr6:166986562-166986612	ProgFib	skin:	n/a
12	chr6:167002977-167003027	HCF	heart:	n/a
13	chr6:166996837-166996887	BJ	skin:	n/a
14	chr6:167011311-167011361	HRCEpiC	kidney:	n/a
15	chr6:166980629-166980679	ECC-1	luminal epithelium:	n/a
16	chr6:166980629-166980679	NHBE	bronchial:	n/a
17	chr6:166984691-166984741	A549	lung:	n/a
18	chr6:166984691-166984741	SK-N-MC	brain:	n/a
19	chr6:166993541-166993591	HRE	kidney:	n/a
20	chr6:166993541-166993591	NH-A	brain:	n/a
21	chr6:167012092-167012142	HRPEpiC	eye:	n/a
22	chr6:166980629-166980679	IMR90	lung:	fetal
23	chr6:166986562-166986612	HCPEpiC	choroid plexus:	n/a
24	chr6:167013972-167014022	NHBE	bronchial:	n/a
25	chr6:166984607-166984657	CMK	blood:	n/a
26	chr6:167011311-167011361	AG09319	gingival:	n/a
27	chr6:167013972-167014022	IMR90	lung:	fetal
28	chr6:167012092-167012142	GM19239	blood:	n/a
29	chr6:166984607-166984657	K562	blood:	n/a
30	chr6:167013972-167014022	HPAEpiC	pulmonary alveolar:	n/a
31	chr6:166984691-166984741	H1-hESC	embryonic stem cell:	embryo
32	chr6:166986562-166986612	HAEpiC	amniotic membrane:	n/a
33	chr6:166984607-166984657	NHBE	bronchial:	n/a
34	chr6:166984691-166984741	HNPCEpiC	eye:	n/a
35	chr6:167011311-167011361	BJ	skin:	n/a
36	chr6:167011311-167011361	SAEC	small airway:	n/a
37	chr6:166986562-166986612	K562	blood:	n/a
38	chr6:167011311-167011361	HCM	heart:	n/a
39	chr6:167012092-167012142	HPAEpiC	pulmonary alveolar:	n/a
40	chr6:166984607-166984657	T-47D	breast:	n/a
41	chr6:166984691-166984741	NHDF-neo	bronchial:	n/a
42	chr6:166984691-166984741	BJ	skin:	n/a
43	chr6:166996837-166996887	MCF-7	breast:	n/a
44	chr6:167011311-167011361	SK-N-SH_RA	brain:	n/a
45	chr6:166993541-166993591	HEK293	kidney:	embryo
46	chr6:166980629-166980679	NB4	blood:	n/a
47	chr6:166993541-166993591	SK-N-SH_RA	brain:	n/a
48	chr6:166984607-166984657	HIPEpiC	eye:	n/a
49	chr6:167012092-167012142	AG04450	lung:	fetal
50	chr6:166993541-166993591	AoSMC	blood vessel:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:166982541..166984779-chr6:166986370..166988271,2	K562	blood:
2	chr6:167005324..167007495-chr6:167014503..167017118,2	MCF-7	breast:
3	chr6:166975267..166978295-chr6:166978843..166980508,3	K562	blood:
4	chr15:91415474..91417592-chr6:166982215..166983716,2	K562	blood:
5	chr6:166982541..166984779-chr6:166986370..166988271,2	K562	blood:
6	chr6:167005324..167007495-chr6:167014503..167017118,2	MCF-7	breast:
7	chr6:166975267..166978295-chr6:166978843..166980508,3	K562	blood:
8	chr6:166974194..166976909-chr6:166977553..166980494,3	K562	blood:
9	chr6:166987161..166988700-chr6:166996130..166998368,2	K562	blood:
10	chr6:166964236..166966556-chr6:166978667..166980857,2	K562	blood:
11	chr6:166987161..166988700-chr6:166996130..166998368,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BRP44L-3	chr6:166999612-166999965	NONHSAT116053

No data

Variant related genes	Relation type
FAM103A2P	TF binding region
FAM103A2P	CpG island
ENSG00000140564	chromatin interactions

Extended variants
information (count: 1652 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1652 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557020453	chr6:166977681-166977682	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs536062086	chr6:166977692-166977693	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142725210	chr6:166977727-166977728	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374363654	chr6:166977740-166977741	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs3799616	chr6:166977753-166977754	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs564752512	chr6:166977806-166977807	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573552336	chr6:166977816-166977817	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192855164	chr6:166977832-166977833	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562025121	chr6:166977833-166977834	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529308625	chr6:166977878-166977879	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560298143	chr6:166977894-166977895	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563039929	chr6:166977940-166977941	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530603530	chr6:166977941-166977942	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552375272	chr6:166977942-166977943	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11963778	chr6:166977944-166977945	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs56318838	chr6:166977983-166977984	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375453872	chr6:166978015-166978016	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569745140	chr6:166978016-166978017	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546498600	chr6:166978086-166978087	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575899415	chr6:166978105-166978106	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537396104	chr6:166978112-166978113	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs11970618	chr6:166978115-166978116	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs556769711	chr6:166978137-166978138	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575329396	chr6:166978138-166978139	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539183087	chr6:166978146-166978147	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558349974	chr6:166978167-166978168	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573488767	chr6:166978168-166978169	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115689594	chr6:166978198-166978199	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555230905	chr6:166978205-166978206	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562414882	chr6:166978233-166978234	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573942531	chr6:166978242-166978243	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372277214	chr6:166978261-166978262	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544629768	chr6:166978291-166978292	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562820605	chr6:166978300-166978301	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78946047	chr6:166978301-166978302	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551473888	chr6:166978311-166978312	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563897175	chr6:166978330-166978331	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185081713	chr6:166978354-166978355	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546484175	chr6:166978382-166978383	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189546182	chr6:166978424-166978425	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535087388	chr6:166978435-166978436	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs59056727	chr6:166978453-166978454	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550576927	chr6:166978467-166978468	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146932736	chr6:166978491-166978492	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73257240	chr6:166978516-166978517	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs576135645	chr6:166978539-166978540	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557892105	chr6:166978601-166978602	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs75368827	chr6:166978650-166978651	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373296838	chr6:166978651-166978652	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs73257242	chr6:166978655-166978656	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:89)

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
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	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
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1275 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166966200-166978000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:166968400-166985800	Weak transcription	Fetal Kidney	kidney
3	chr6:166969400-166978800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:166970800-166979800	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr6:166970800-166986200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:166971000-166986000	Weak transcription	Pancreas	Pancrea
7	chr6:166971400-166980200	Weak transcription	Brain Anterior Caudate	brain
8	chr6:166972200-166979600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr6:166972200-166986000	Weak transcription	Gastric	stomach
10	chr6:166972400-166979200	Weak transcription	NHEK	skin
11	chr6:166973000-166979200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:166973400-166984600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:166973600-166978000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr6:166973800-166979000	Weak transcription	HMEC	breast
15	chr6:166973800-166979200	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr6:166973800-166986000	Weak transcription	Fetal Intestine Small	intestine
17	chr6:166974000-166978400	Weak transcription	Stomach Smooth Muscle	stomach
18	chr6:166974000-166979400	Weak transcription	Brain Substantia Nigra	brain
19	chr6:166974000-166989600	Weak transcription	Primary T cells from cord blood	blood
20	chr6:166974200-166981600	Enhancers	Fetal Muscle Leg	muscle
21	chr6:166974400-166978400	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr6:166974400-166992400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr6:166974600-166977800	Enhancers	Spleen	Spleen
24	chr6:166974600-166978000	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr6:166974600-166979000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr6:166974600-166979400	Genic enhancers	Fetal Stomach	stomach
27	chr6:166974600-166981000	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr6:166974800-166986000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr6:166975000-166979200	Weak transcription	Brain Angular Gyrus	brain
30	chr6:166975600-166979400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr6:166975600-166981600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr6:166975800-166979000	Weak transcription	Brain Cingulate Gyrus	brain
33	chr6:166975800-166979600	Weak transcription	HSMM	muscle
34	chr6:166975800-166980000	Weak transcription	Osteobl	bone
35	chr6:166976000-166978000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr6:166976000-166978200	Weak transcription	Rectal Smooth Muscle	rectum
37	chr6:166976000-166979000	Weak transcription	HSMMtube	muscle
38	chr6:166976200-166978000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:166976200-166978800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr6:166976200-166981600	Enhancers	Fetal Muscle Trunk	muscle
41	chr6:166976400-166978200	Weak transcription	NHLF	lung
42	chr6:166976400-166978400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr6:166976400-166979600	Weak transcription	NHDF-Ad	bronchial
44	chr6:166976400-166988600	Weak transcription	Ovary	ovary
45	chr6:166976600-166978200	Enhancers	H1 Cell Line	embryonic stem cell
46	chr6:166976600-166978400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr6:166976600-166979000	Weak transcription	Right Atrium	heart
48	chr6:166976600-166979600	Weak transcription	Right Ventricle	heart
49	chr6:166976800-166977800	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr6:166976800-166978800	Weak transcription	Psoas Muscle	Psoas

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