Variant report

Variant	nsv886942
Chromosome Location	chr6:167245665-167282950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:424)
CpG islands
(count:1651)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167264235-167264605	K562	blood:	n/a	n/a
2	ATF1	chr6:167264121-167264564	K562	blood:	n/a	n/a
3	ATF1	chr6:167260351-167260433	K562	blood:	n/a	n/a
4	ATF1	chr6:167255068-167255231	K562	blood:	n/a	n/a
5	ATF2	chr6:167247521-167247974	GM12878	blood:	n/a	n/a
6	ATF2	chr6:167263194-167263607	GM12878	blood:	n/a	n/a
7	ATF2	chr6:167247492-167247983	GM12878	blood:	n/a	n/a
8	BACH1	chr6:167276270-167276880	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr6:167263166-167263351	GM12878	blood:	n/a	n/a
10	BATF	chr6:167247594-167247848	GM12878	blood:	n/a	n/a
11	BATF	chr6:167263100-167263391	GM12878	blood:	n/a	n/a
12	BATF	chr6:167247528-167247858	GM12878	blood:	n/a	n/a
13	BCLAF1	chr6:167247514-167247888	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:167256306-167256412	K562	blood:	n/a	n/a
15	BHLHE40	chr6:167276161-167276327	GM12878	blood:	n/a	n/a
16	BHLHE40	chr6:167263347-167263548	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:167264030-167264513	K562	blood:	n/a	n/a
18	BHLHE40	chr6:167247873-167248126	GM12878	blood:	n/a	n/a
19	CBX3	chr6:167264115-167264437	K562	blood:	n/a	n/a
20	CCNT2	chr6:167264000-167264442	K562	blood:	n/a	chr6:167264339-167264359
21	CCNT2	chr6:167254977-167255146	K562	blood:	n/a	n/a
22	CEBPB	chr6:167269019-167269228	K562	blood:	n/a	n/a
23	CEBPB	chr6:167269110-167269239	A549	lung:	n/a	n/a
24	CEBPB	chr6:167248017-167248058	A549	lung:	n/a	n/a
25	CEBPB	chr6:167246565-167246688	A549	lung:	n/a	n/a
26	CEBPB	chr6:167269010-167269276	HepG2	liver:	n/a	n/a
27	CEBPD	chr6:167245206-167245696	K562	blood:	n/a	n/a
28	CHD1	chr6:167275559-167276071	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr6:167272213-167272327	GM12878	blood:	n/a	n/a
30	CHD2	chr6:167276445-167276497	GM12878	blood:	n/a	n/a
31	CHD2	chr6:167275963-167276282	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr6:167266280-167266430	GM12872	blood:	n/a	n/a
33	CTCF	chr6:167250860-167251010	GM06990	blood:	n/a	chr6:167250996-167251009 chr6:167250950-167250971
34	CTCF	chr6:167267180-167267330	HEK293	kidney:	n/a	chr6:167267208-167267216
35	CTCF	chr6:167266320-167266470	GM12875	blood:	n/a	n/a
36	CTCF	chr6:167276200-167276350	HMF	breast:	n/a	chr6:167276287-167276300
37	CTCF	chr6:167275740-167275890	SK-N-SH_RA	brain:	n/a	chr6:167275777-167275790 chr6:167275774-167275792
38	CTCF	chr6:167250860-167251010	HepG2	liver:	n/a	chr6:167250996-167251009 chr6:167250950-167250971
39	CTCF	chr6:167250920-167251070	Caco-2	colon:	n/a	chr6:167250996-167251009 chr6:167250950-167250971
40	CTCF	chr6:167276233-167276398	H1-hESC	embryonic stem cell:	n/a	chr6:167276287-167276300
41	CTCF	chr6:167276220-167276370	WERI-Rb-1	eye:	n/a	chr6:167276287-167276300
42	CTCF	chr6:167276158-167276444	GM12891	blood:	n/a	chr6:167276287-167276300
43	CTCF	chr6:167276254-167276387	Spleen_OC	spleen:	n/a	chr6:167276287-167276300
44	CTCF	chr6:167250914-167251092	K562	blood:	n/a	chr6:167250996-167251009 chr6:167250950-167250971
45	CTCF	chr6:167266280-167266430	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr6:167276200-167276350	GM12864	blood:	n/a	chr6:167276287-167276300
47	CTCF	chr6:167276226-167276350	SK-N-SH_RA	brain:	n/a	chr6:167276287-167276300
48	CTCF	chr6:167275780-167275930	BE2_C	brain:	n/a	n/a
49	CTCF	chr6:167276220-167276370	HRE	kidney:	n/a	chr6:167276287-167276300
50	CTCF	chr6:167276260-167276410	GM12872	blood:	n/a	chr6:167276287-167276300

(count:1651 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167275684-167275734	LNCaP	prostate:	n/a
2	chr6:167275999-167276049	CMK	blood:	n/a
3	chr6:167275999-167276049	Hepatocyte	liver:	n/a
4	chr6:167275755-167275805	HIPEpiC	eye:	n/a
5	chr6:167275684-167275734	LNCaP	prostate:	n/a
6	chr6:167275999-167276049	CMK	blood:	n/a
7	chr6:167275999-167276049	Hepatocyte	liver:	n/a
8	chr6:167275755-167275805	HIPEpiC	eye:	n/a
9	chr6:167250429-167250479	NHBE	bronchial:	n/a
10	chr6:167275832-167275882	HMEC	breast:	n/a
11	chr6:167276275-167276325	GM12878	blood:	n/a
12	chr6:167275395-167275445	AG10803	skin:	n/a
13	chr6:167263225-167263275	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:167275781-167275831	HAEpiC	amniotic membrane:	n/a
15	chr6:167271883-167271933	IMR90	lung:	fetal
16	chr6:167275999-167276049	SAEC	small airway:	n/a
17	chr6:167276359-167276409	Hepatocyte	liver:	n/a
18	chr6:167276567-167276617	HAEpiC	amniotic membrane:	n/a
19	chr6:167263025-167263075	HRE	kidney:	n/a
20	chr6:167276275-167276325	HRE	kidney:	n/a
21	chr6:167263066-167263116	PrEC	prostate:	n/a
22	chr6:167276275-167276325	BE2_C	brain:	n/a
23	chr6:167250541-167250591	U87	brain:	n/a
24	chr6:167275395-167275445	RPTEC	kidney:	n/a
25	chr6:167276359-167276409	LNCaP	prostate:	n/a
26	chr6:167263193-167263243	HepG2	liver:	n/a
27	chr6:167275684-167275734	GM12891	blood:	n/a
28	chr6:167263401-167263451	Jurkat	blood:	n/a
29	chr6:167275999-167276049	H1-hESC	embryonic stem cell:	embryo
30	chr6:167276650-167276700	ovcar-3	ovarian:	n/a
31	chr6:167250541-167250591	HRE	kidney:	n/a
32	chr6:167275843-167275893	HEEpiC	esophagus:	n/a
33	chr6:167250541-167250591	GM19239	blood:	n/a
34	chr6:167276275-167276325	ovcar-3	ovarian:	n/a
35	chr6:167263193-167263243	MCF-7	breast:	n/a
36	chr6:167263401-167263451	NH-A	brain:	n/a
37	chr6:167275755-167275805	AG10803	skin:	n/a
38	chr6:167275809-167275859	HNPCEpiC	eye:	n/a
39	chr6:167280873-167280923	MCF10A-Er-Src	breast:	n/a
40	chr6:167263225-167263275	HCT-116	colon:	n/a
41	chr6:167275755-167275805	BJ	skin:	n/a
42	chr6:167263225-167263275	LNCaP	prostate:	n/a
43	chr6:167276650-167276700	HL-60	blood:	n/a
44	chr6:167275832-167275882	GM12891	blood:	n/a
45	chr6:167275755-167275805	BE2_C	brain:	n/a
46	chr6:167275781-167275831	ovcar-3	ovarian:	n/a
47	chr6:167279026-167279076	SK-N-SH_RA	brain:	n/a
48	chr6:167275778-167275828	BJ	skin:	n/a
49	chr6:167271883-167271933	AG09309	skin:	n/a
50	chr6:167276567-167276617	PFSK-1	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:167244883..167247077-chr6:167250402..167252258,2	K562	blood:
2	chr6:167274608..167276505-chr6:167368344..167370567,2	MCF-7	breast:
3	chr6:167263153..167265718-chr6:167272365..167274771,2	K562	blood:
4	chr6:167244459..167246952-chr6:167353805..167356355,2	K562	blood:
5	chr6:167268417..167269941-chr6:167289089..167292061,2	K562	blood:
6	chr6:167280811..167283547-chr6:167284862..167287593,2	K562	blood:
7	chr6:167244883..167247077-chr6:167250402..167252258,2	K562	blood:
8	chr6:167266120..167268418-chr6:167368019..167370456,2	K562	blood:
9	chr6:167263153..167265718-chr6:167272365..167274771,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGFR1OP-10	chr6:167254947-167255400	l_3320_chr6:167242351-167255400_testes

No data

Variant related genes	Relation type
RPS6KA2	TF binding region
RPS6KA2	CpG island
ENSG00000026297	chromatin interactions
ENSG00000249141	chromatin interactions

Extended variants
information (count: 1636 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1636 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9355598	chr6:167245665-167245666	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189547103	chr6:167245672-167245673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs9356518	chr6:167245725-167245726	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs552654912	chr6:167245762-167245763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs137918566	chr6:167245798-167245799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs74784344	chr6:167245916-167245917	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs557568441	chr6:167245953-167245954	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs183325770	chr6:167246024-167246025	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs78960679	chr6:167246119-167246120	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs75539067	chr6:167246124-167246125	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs573281462	chr6:167246189-167246190	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs540582977	chr6:167246254-167246255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562185191	chr6:167246305-167246306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs143872721	chr6:167246364-167246365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544363473	chr6:167246386-167246387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563524862	chr6:167246389-167246390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76461684	chr6:167246414-167246415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373651391	chr6:167246433-167246434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552456683	chr6:167246449-167246450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563992356	chr6:167246493-167246494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368039195	chr6:167246569-167246570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368206650	chr6:167246635-167246636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556755919	chr6:167246646-167246647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528098076	chr6:167246673-167246674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575383409	chr6:167246674-167246675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546156406	chr6:167246701-167246702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536375638	chr6:167246709-167246710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567705211	chr6:167246718-167246719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187065209	chr6:167246740-167246741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140203688	chr6:167246751-167246752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555045351	chr6:167246759-167246760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79516527	chr6:167246765-167246766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192193774	chr6:167246784-167246785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7745781	chr6:167246816-167246817	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs558563296	chr6:167246925-167246926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540641186	chr6:167246943-167246944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113522483	chr6:167246959-167246960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555830645	chr6:167246983-167246984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370561325	chr6:167247000-167247001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560351996	chr6:167247017-167247018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530151316	chr6:167247042-167247043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9364874	chr6:167247046-167247047	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs562802172	chr6:167247049-167247050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375816458	chr6:167247050-167247051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575399673	chr6:167247106-167247107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545566099	chr6:167247112-167247113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564057697	chr6:167247137-167247138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78969777	chr6:167247139-167247140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546469938	chr6:167247147-167247148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561396109	chr6:167247168-167247169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Autism	22549408	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:524 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167244400-167253800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr6:167244800-167253600	Weak transcription	Primary B cells from peripheral blood	blood
3	chr6:167245000-167250400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:167245200-167245800	Enhancers	GM12878-XiMat	blood
5	chr6:167245600-167245800	Enhancers	Fetal Stomach	stomach
6	chr6:167245800-167246200	ZNF genes & repeats	GM12878-XiMat	blood
7	chr6:167249000-167272200	Weak transcription	Fetal Stomach	stomach
8	chr6:167250400-167250600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:167250400-167251000	Enhancers	H1 Cell Line	embryonic stem cell
10	chr6:167250400-167251200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:167250600-167251200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:167251000-167251800	Enhancers	Stomach Smooth Muscle	stomach
13	chr6:167251200-167251800	Enhancers	Fetal Brain Male	brain
14	chr6:167251200-167266000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:167251600-167251800	Enhancers	Brain Substantia Nigra	brain
16	chr6:167251800-167252600	Weak transcription	Brain Substantia Nigra	brain
17	chr6:167251800-167272800	Weak transcription	Stomach Smooth Muscle	stomach
18	chr6:167252200-167252400	Enhancers	Fetal Muscle Trunk	muscle
19	chr6:167252200-167252600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr6:167252400-167252600	Enhancers	Left Ventricle	heart
21	chr6:167252400-167253000	Enhancers	Brain Anterior Caudate	brain
22	chr6:167252400-167253000	Weak transcription	Fetal Muscle Trunk	muscle
23	chr6:167252600-167252800	Enhancers	Brain Substantia Nigra	brain
24	chr6:167252600-167253600	Weak transcription	Left Ventricle	heart
25	chr6:167252800-167253600	Weak transcription	Brain Substantia Nigra	brain
26	chr6:167253000-167254000	Enhancers	Fetal Muscle Trunk	muscle
27	chr6:167253000-167265400	Weak transcription	Brain Anterior Caudate	brain
28	chr6:167253200-167255600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr6:167253600-167253800	Enhancers	Brain Angular Gyrus	brain
30	chr6:167253600-167253800	Enhancers	Brain Substantia Nigra	brain
31	chr6:167253600-167254000	Enhancers	Primary B cells from peripheral blood	blood
32	chr6:167253600-167254000	Enhancers	Left Ventricle	heart
33	chr6:167253600-167254000	Enhancers	GM12878-XiMat	blood
34	chr6:167253800-167254000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
35	chr6:167253800-167256600	Weak transcription	Brain Substantia Nigra	brain
36	chr6:167253800-167263200	Weak transcription	Brain Angular Gyrus	brain
37	chr6:167255600-167257000	Bivalent Enhancer	K562	blood
38	chr6:167256600-167256800	Enhancers	Brain Substantia Nigra	brain
39	chr6:167259800-167260400	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr6:167260000-167260600	Enhancers	Primary B cells from cord blood	blood
41	chr6:167260000-167260800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr6:167260000-167261000	Enhancers	Primary B cells from peripheral blood	blood
43	chr6:167260200-167260400	Flanking Active TSS	Small Intestine	intestine
44	chr6:167260200-167260400	Enhancers	GM12878-XiMat	blood
45	chr6:167260400-167274400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr6:167260600-167262400	Weak transcription	GM12878-XiMat	blood
47	chr6:167260600-167262600	Weak transcription	Primary B cells from cord blood	blood
48	chr6:167261000-167262000	Weak transcription	Primary B cells from peripheral blood	blood
49	chr6:167262000-167264400	Enhancers	Primary B cells from peripheral blood	blood
50	chr6:167262000-167264600	Weak transcription	Brain Cingulate Gyrus	brain

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