Variant report

Variant	nsv462899
Chromosome Location	chr6:33880480-33944014
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:95)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:95 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:33906140..33909513-chr6:33910845..33914696,4	MCF-7	breast:
2	chr6:33935012..33937459-chr6:33942472..33944353,2	K562	blood:
3	chr6:33935012..33937286-chr6:33941317..33943972,2	K562	blood:
4	chr6:33913220..33915544-chr6:33919122..33921053,3	K562	blood:
5	chr6:33881960..33884632-chr6:33890254..33892138,2	MCF-7	breast:
6	chr6:33889301..33891295-chr6:33893336..33896618,3	MCF-7	breast:
7	chr6:33885575..33887845-chr6:33891756..33894139,2	MCF-7	breast:
8	chr6:33918842..33920880-chr6:33924191..33925775,2	K562	blood:
9	chr6:33919883..33922480-chr6:33924256..33927487,4	MCF-7	breast:
10	chr6:33916864..33919171-chr6:33930801..33933029,2	MCF-7	breast:
11	chr6:33935782..33936335-chr6:33955656..33956622,2	MCF-7	breast:
12	chr6:33942809..33944696-chr6:33949318..33951158,2	MCF-7	breast:
13	chr6:33935685..33937732-chr6:33955927..33958373,2	MCF-7	breast:
14	chr6:33868116..33871779-chr6:33880960..33883614,3	K562	blood:
15	chr6:33897589..33900344-chr6:33900487..33902358,2	K562	blood:
16	chr6:33881007..33883115-chr6:33890110..33892674,2	MCF-7	breast:
17	chr6:33922283..33924139-chr6:33925497..33927060,2	K562	blood:
18	chr6:33927135..33929143-chr6:33944981..33947651,2	MCF-7	breast:
19	chr6:33875969..33877770-chr6:33880104..33881906,2	K562	blood:
20	chr6:33913064..33919897-chr6:33920862..33926806,7	K562	blood:
21	chr6:33877120..33879960-chr6:33887589..33889493,2	K562	blood:
22	chr6:33906140..33909513-chr6:33910845..33914696,4	MCF-7	breast:
23	chr6:33890903..33893411-chr6:33904076..33906137,2	MCF-7	breast:
24	chr6:33906340..33908280-chr6:33915732..33918337,2	K562	blood:
25	chr6:33899516..33901921-chr6:33904882..33906731,2	K562	blood:
26	chr6:33870279..33872339-chr6:33881420..33883614,2	K562	blood:
27	chr6:33887758..33891673-chr6:33891780..33895604,5	K562	blood:
28	chr6:33892310..33894285-chr6:33898684..33900893,3	K562	blood:
29	chr6:33912597..33914760-chr6:33916307..33917963,2	MCF-7	breast:
30	chr6:33896064..33898965-chr6:33913599..33916267,2	MCF-7	breast:
31	chr6:33896064..33898965-chr6:33913599..33916267,2	MCF-7	breast:
32	chr6:33906156..33908809-chr6:33914249..33915924,2	MCF-7	breast:
33	chr6:33908656..33910673-chr6:34085425..34087423,2	K562	blood:
34	chr6:33881960..33884632-chr6:33890254..33892138,2	MCF-7	breast:
35	chr6:33912597..33914760-chr6:33916307..33917963,2	MCF-7	breast:
36	chr6:33934133..33938274-chr6:33943444..33948778,6	MCF-7	breast:
37	chr6:33928847..33930667-chr6:33930699..33932351,2	K562	blood:
38	chr6:33928175..33930963-chr6:33993122..33995355,2	MCF-7	breast:
39	chr6:33893477..33895597-chr6:33913163..33915930,2	K562	blood:
40	chr6:33893792..33896419-chr6:33908700..33911683,2	K562	blood:
41	chr6:33893477..33895597-chr6:33913163..33915930,2	K562	blood:
42	chr6:33892310..33894351-chr6:33897735..33900618,2	K562	blood:
43	chr6:33912394..33915055-chr6:33946729..33949481,2	MCF-7	breast:
44	chr6:33897453..33899504-chr6:33914430..33916808,2	K562	blood:
45	chr6:33918842..33920880-chr6:33924191..33925775,2	K562	blood:
46	chr6:33875835..33878450-chr6:33882484..33884000,2	K562	blood:
47	chr6:33935283..33936415-chr6:33994982..33996031,6	MCF-7	breast:
48	chr6:33925599..33928278-chr6:33928837..33930807,2	K562	blood:
49	chr6:33878954..33881384-chr6:33881544..33883413,2	MCF-7	breast:
50	chr6:33936123..33939292-chr6:33941917..33944139,3	MCF-7	breast:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ITPR3-1	chr6:33892111-33895408	ENSG00000233183
2	lnc-ITPR3-1	chr6:33888703-33888791	ENSG00000233183
3	lnc-ITPR3-1	chr6:33882503-33885984	XLOC_005263
4	lnc-ITPR3-1	chr6:33882503-33882612	XLOC_005263
5	lnc-ITPR3-1	chr6:33881865-33883172	NONHSAT109994
6	lnc-ITPR3-1	chr6:33878879-33881988	ENSG00000233183
7	lnc-ITPR3-1	chr6:33880996-33881988	NONHSAT111951
8	lnc-ITPR3-1	chr6:33881865-33881988	XLOC_005263
9	lnc-ITPR3-1	chr6:33881865-33881988	XLOC_005263
10	lnc-ITPR3-1	chr6:33881861-33881988	XLOC_005263
11	lnc-ITPR3-1	chr6:33882503-33885968	XLOC_005263
12	lnc-ITPR3-1	chr6:33892111-33892460	XLOC_005263
13	lnc-ITPR3-1	chr6:33882503-33885985	ENSG00000233183
14	lnc-ITPR3-1	chr6:33881865-33881988	XLOC_005263
15	lnc-ITPR3-1	chr6:33882234-33882612	XLOC_005263
16	lnc-ITPR3-1	chr6:33882234-33883172	NONHSAT111951
17	lnc-ITPR3-1	chr6:33888703-33888791	XLOC_005263
18	lnc-ITPR3-1	chr6:33881865-33882187	ENSG00000233183
19	lnc-ITPR3-1	chr6:33878879-33881988	XLOC_005263
20	lnc-ITPR3-1	chr6:33881865-33881988	XLOC_005263
21	lnc-ITPR3-1	chr6:33881865-33881988	XLOC_005263
22	lnc-ITPR3-1	chr6:33882503-33882612	XLOC_005263
23	lnc-ITPR3-1	chr6:33881865-33881988	ENSG00000233183
24	lnc-ITPR3-1	chr6:33882234-33885968	XLOC_005263

No data

Variant related genes	Relation type
ENSG00000233183	chromatin interactions
ENSG00000161904	chromatin interactions
CANT1	miRNA target sites
IL6R	miRNA target sites
CANX	miRNA target sites

Extended variants
information (count: 2709 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2709 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12191571	chr6:33880480-33880481	Weak transcription Enhancers Bivalent Enhancer	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553879638	chr6:33880490-33880491	Weak transcription Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
3	rs572461364	chr6:33880491-33880492	Weak transcription Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
4	rs75460681	chr6:33880585-33880586	Weak transcription Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
5	rs561141505	chr6:33880662-33880663	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs531814093	chr6:33880717-33880718	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs543693000	chr6:33880755-33880756	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs146446591	chr6:33880757-33880758	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs188314608	chr6:33880777-33880778	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs191293881	chr6:33880778-33880779	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs547329073	chr6:33880803-33880804	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs565581434	chr6:33880808-33880809	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs72887201	chr6:33880812-33880813	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs138737206	chr6:33880827-33880828	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs548334342	chr6:33880841-33880842	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs569852575	chr6:33880849-33880850	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs370042123	chr6:33880867-33880868	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs6930602	chr6:33880904-33880905	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs183878315	chr6:33880998-33880999	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs4713721	chr6:33881017-33881018	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs570675709	chr6:33881025-33881026	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs534621701	chr6:33881057-33881058	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs9461927	chr6:33881059-33881060	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs572394621	chr6:33881067-33881068	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs536324065	chr6:33881073-33881074	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs369343922	chr6:33881082-33881083	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs553345495	chr6:33881104-33881105	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs576143376	chr6:33881129-33881130	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs189641302	chr6:33881183-33881184	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs75912547	chr6:33881207-33881208	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs577458163	chr6:33881299-33881300	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs568344516	chr6:33881309-33881310	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs181768933	chr6:33881322-33881323	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs375271346	chr6:33881370-33881371	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs559280988	chr6:33881386-33881387	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs34810309	chr6:33881415-33881416	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs186878504	chr6:33881426-33881427	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs548225963	chr6:33881447-33881448	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs563346020	chr6:33881504-33881505	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs398001102	chr6:33881508-33881509	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs556833504	chr6:33881521-33881522	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs9469625	chr6:33881570-33881571	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs552358072	chr6:33881605-33881606	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs570594163	chr6:33881612-33881613	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs190617001	chr6:33881666-33881667	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs546605738	chr6:33881707-33881708	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs147358918	chr6:33881713-33881714	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs182044825	chr6:33881795-33881796	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs79756150	chr6:33881804-33881805	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs9469626	chr6:33881862-33881863	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD

Chromatin state (count:527 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33865600-33883000	Weak transcription	Esophagus	oesophagus
2	chr6:33873000-33884000	Enhancers	Fetal Thymus	thymus
3	chr6:33873400-33883800	Enhancers	Primary T cells fromperipheralblood	blood
4	chr6:33873800-33882000	Weak transcription	Spleen	Spleen
5	chr6:33874000-33881800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr6:33874200-33882200	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr6:33874200-33889200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:33875400-33881400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr6:33875400-33881400	Weak transcription	Thymus	Thymus
10	chr6:33876000-33880800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr6:33876600-33881800	Weak transcription	Primary B cells from cord blood	blood
12	chr6:33876600-33882000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr6:33876800-33882000	Weak transcription	GM12878-XiMat	blood
14	chr6:33877000-33881600	Weak transcription	Primary T cells from cord blood	blood
15	chr6:33877800-33881400	Weak transcription	Primary hematopoietic stem cells	blood
16	chr6:33878000-33883600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr6:33878400-33883200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr6:33879400-33881200	Enhancers	Colon Smooth Muscle	Colon
19	chr6:33879600-33880600	Enhancers	Rectal Smooth Muscle	rectum
20	chr6:33879600-33880800	Enhancers	Duodenum Smooth Muscle	Duodenum
21	chr6:33879800-33881000	Enhancers	Stomach Smooth Muscle	stomach
22	chr6:33879800-33883800	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr6:33879800-33883800	Enhancers	Fetal Stomach	stomach
24	chr6:33880000-33880600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
25	chr6:33880000-33881000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr6:33880000-33882000	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr6:33880000-33882200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr6:33880000-33882400	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr6:33880400-33880800	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr6:33880400-33882200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr6:33880400-33883000	Weak transcription	Fetal Lung	lung
32	chr6:33880600-33882200	Weak transcription	Rectal Smooth Muscle	rectum
33	chr6:33880600-33883200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr6:33880800-33882400	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr6:33880800-33882600	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr6:33880800-33883800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr6:33881000-33883800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr6:33881200-33882600	Weak transcription	Colon Smooth Muscle	Colon
39	chr6:33881200-33884000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr6:33881400-33883400	Enhancers	Thymus	Thymus
41	chr6:33881400-33883600	Enhancers	Primary hematopoietic stem cells	blood
42	chr6:33881400-33883600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr6:33881400-33883800	Enhancers	Primary B cells from peripheral blood	blood
44	chr6:33881600-33882000	Enhancers	Primary T cells from cord blood	blood
45	chr6:33881600-33883400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
46	chr6:33881800-33882200	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr6:33881800-33883000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr6:33881800-33883400	Enhancers	Primary B cells from cord blood	blood
49	chr6:33882000-33882200	Enhancers	Duodenum Mucosa	Duodenum
50	chr6:33882000-33882200	Enhancers	Sigmoid Colon	Sigmoid Colon

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