Variant report

Variant	esv2757476
Chromosome Location	chr11:107324276-107344568
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:453)
CpG islands
(count:794)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:107328127-107328887	K562	blood:	n/a	n/a
2	ARID3A	chr11:107328280-107328788	HepG2	liver:	n/a	n/a
3	ATF1	chr11:107328463-107328763	K562	blood:	n/a	n/a
4	ATF2	chr11:107328307-107328946	GM12878	blood:	n/a	n/a
5	ATF3	chr11:107328243-107328841	HepG2	liver:	n/a	n/a
6	ATF3	chr11:107328375-107328670	K562	blood:	n/a	n/a
7	ATF3	chr11:107328394-107328774	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr11:107328335-107328738	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr11:107328369-107328693	GM12878	blood:	n/a	n/a
10	ATF3	chr11:107328396-107328669	HepG2	liver:	n/a	n/a
11	ATF3	chr11:107328251-107328813	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:107328231-107328803	K562	blood:	n/a	n/a
13	BRCA1	chr11:107328002-107328799	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr11:107339406-107339761	K562	blood:	n/a	n/a
15	CBX3	chr11:107328281-107328798	K562	blood:	n/a	n/a
16	CCNT2	chr11:107328454-107328790	K562	blood:	n/a	n/a
17	CEBPB	chr11:107326821-107327385	HepG2	liver:	n/a	n/a
18	CEBPB	chr11:107339344-107339654	K562	blood:	n/a	n/a
19	CEBPB	chr11:107328347-107328697	K562	blood:	n/a	n/a
20	CREB1	chr11:107328330-107328824	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr11:107328500-107328650	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr11:107328364-107328659	Lung_OC	lung:	n/a	n/a
23	CTCF	chr11:107328460-107328610	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr11:107328421-107328677	Spleen_OC	spleen:	n/a	n/a
25	CTCF	chr11:107328640-107328790	HPF	lung:	n/a	n/a
26	CTCF	chr11:107339480-107339630	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr11:107328200-107328350	Caco-2	colon:	n/a	n/a
28	CTCF	chr11:107328460-107328610	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr11:107328600-107328750	AG09309	skin:	n/a	n/a
30	CTCF	chr11:107328613-107328688	LNCaP	prostate:	n/a	n/a
31	CTCF	chr11:107328840-107328990	AG04450	lung:	n/a	n/a
32	CTCF	chr11:107329780-107329930	Caco-2	colon:	n/a	n/a
33	CTCF	chr11:107328420-107328570	SAEC	small airway:	n/a	n/a
34	CTCF	chr11:107328567-107328709	GM19240	blood:	n/a	n/a
35	CTCF	chr11:107328647-107328673	GM13977	blood:	n/a	n/a
36	CTCF	chr11:107328860-107329010	GM12864	blood:	n/a	n/a
37	CTCF	chr11:107328500-107328650	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr11:107328400-107328550	HepG2	liver:	n/a	n/a
39	CTCF	chr11:107339579-107339725	K562	blood:	n/a	n/a
40	CTCF	chr11:107328500-107328650	AG09319	gingival:	n/a	n/a
41	CTCF	chr11:107328420-107328570	HRE	kidney:	n/a	n/a
42	CTCF	chr11:107328480-107328630	AG09319	gingival:	n/a	n/a
43	CTCF	chr11:107328440-107328590	BE2_C	brain:	n/a	n/a
44	CTCF	chr11:107339600-107339750	HMEC	breast:	n/a	n/a
45	CTCF	chr11:107328360-107328510	HRE	kidney:	n/a	n/a
46	CTCF	chr11:107328456-107328540	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr11:107329760-107329910	HCT-116	colon:	n/a	n/a
48	CTCF	chr11:107328360-107328510	HAc	cerebellar:	n/a	n/a
49	CTCF	chr11:107328480-107328630	AG10803	skin:	n/a	n/a
50	CTCF	chr11:107328600-107328750	HCM	heart:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:107331110-107331160	AG09319	gingival:	n/a
2	chr11:107331110-107331160	AG09319	gingival:	n/a
3	chr11:107328559-107328609	Caco-2	colon:	n/a
4	chr11:107328914-107328964	IMR90	lung:	fetal
5	chr11:107328914-107328964	T-47D	breast:	n/a
6	chr11:107328657-107328707	AG09309	skin:	n/a
7	chr11:107328671-107328721	SAEC	small airway:	n/a
8	chr11:107328690-107328740	HCT-116	colon:	n/a
9	chr11:107331110-107331160	BE2_C	brain:	n/a
10	chr11:107328657-107328707	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:107328636-107328686	H1-hESC	embryonic stem cell:	embryo
12	chr11:107328636-107328686	SKMC	muscle:	n/a
13	chr11:107328586-107328636	AG09309	skin:	n/a
14	chr11:107328605-107328655	MCF10A-Er-Src	breast:	n/a
15	chr11:107328690-107328740	AG09319	gingival:	n/a
16	chr11:107324751-107324801	MCF10A-Er-Src	breast:	n/a
17	chr11:107328671-107328721	LNCaP	prostate:	n/a
18	chr11:107328586-107328636	Jurkat	blood:	n/a
19	chr11:107328914-107328964	NHBE	bronchial:	n/a
20	chr11:107328605-107328655	ovcar-3	ovarian:	n/a
21	chr11:107328671-107328721	CMK	blood:	n/a
22	chr11:107328690-107328740	HIPEpiC	eye:	n/a
23	chr11:107331110-107331160	HUVEC	blood vessel:	n/a
24	chr11:107328657-107328707	GM12892	blood:	n/a
25	chr11:107328690-107328740	GM12891	blood:	n/a
26	chr11:107328914-107328964	SAEC	small airway:	n/a
27	chr11:107328605-107328655	Hepatocyte	liver:	n/a
28	chr11:107328442-107328492	Hela-S3	cervix:	n/a
29	chr11:107328690-107328740	PANC-1	pancreas:	n/a
30	chr11:107328636-107328686	GM12878	blood:	n/a
31	chr11:107328525-107328575	HCPEpiC	choroid plexus:	n/a
32	chr11:107328690-107328740	ECC-1	luminal epithelium:	n/a
33	chr11:107328657-107328707	CMK	blood:	n/a
34	chr11:107328636-107328686	GM19239	blood:	n/a
35	chr11:107328559-107328609	AoSMC	blood vessel:	n/a
36	chr11:107328690-107328740	AoSMC	blood vessel:	n/a
37	chr11:107324751-107324801	AG09319	gingival:	n/a
38	chr11:107328525-107328575	HAEpiC	amniotic membrane:	n/a
39	chr11:107328671-107328721	GM12878	blood:	n/a
40	chr11:107328914-107328964	NHDF-neo	bronchial:	n/a
41	chr11:107328657-107328707	SK-N-SH_RA	brain:	n/a
42	chr11:107328636-107328686	HEEpiC	esophagus:	n/a
43	chr11:107328657-107328707	Jurkat	blood:	n/a
44	chr11:107326471-107326521	GM19239	blood:	n/a
45	chr11:107328914-107328964	K562	blood:	n/a
46	chr11:107328586-107328636	HCF	heart:	n/a
47	chr11:107328671-107328721	T-47D	breast:	n/a
48	chr11:107328657-107328707	HRE	kidney:	n/a
49	chr11:107328914-107328964	HCM	heart:	n/a
50	chr11:107324751-107324801	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr11:107311896..107313858-chr11:107327138..107329604,2	K562	blood:
2	chr1:28908024..28908798-chr11:107328064..107328889,2	HCT-116	colon:
3	chr11:107321712..107323606-chr11:107324966..107327081,2	K562	blood:
4	chr11:107321712..107324920-chr11:107324966..107329578,5	K562	blood:
5	chr11:107328376..107329012-chr20:10654520..10655433,2	HCT-116	colon:
6	chr11:107317031..107320685-chr11:107326705..107328538,3	K562	blood:
7	chr11:107317620..107320783-chr11:107322990..107325407,3	K562	blood:
8	chr11:107321719..107323399-chr11:107326158..107328000,2	MCF-7	breast:
9	chr11:107342962..107345043-chr11:107346726..107348566,2	K562	blood:

No data

Variant related genes	Relation type
CWF19L2	TF binding region
CWF19L2	CpG island
ENSG00000101384	chromatin interactions
ENSG00000152404	chromatin interactions
ENSG00000197989	chromatin interactions

Extended variants
information (count: 250 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:250 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs476028	chr11:107324276-107324277	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531585759	chr11:107324306-107324307	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs34358550	chr11:107324308-107324309	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs78002743	chr11:107324329-107324330	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs11212249	chr11:107324338-107324339	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs11212250	chr11:107324344-107324345	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs185120555	chr11:107324399-107324400	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs34832476	chr11:107324406-107324407	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs555652476	chr11:107324432-107324433	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs373484655	chr11:107324469-107324470	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs149580638	chr11:107324517-107324518	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs73549883	chr11:107324621-107324622	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs555935396	chr11:107324719-107324720	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs147266032	chr11:107324752-107324753	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs78617779	chr11:107324830-107324831	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs559768067	chr11:107324846-107324847	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs375326670	chr11:107324871-107324872	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs189247840	chr11:107324880-107324881	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs547966323	chr11:107324889-107324890	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs542818341	chr11:107324947-107324948	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561515531	chr11:107324968-107324969	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs627440	chr11:107324991-107324992	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs139173571	chr11:107325075-107325076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11212251	chr11:107325125-107325126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571560694	chr11:107325203-107325204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532502837	chr11:107325261-107325262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547934221	chr11:107325287-107325288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181139422	chr11:107325309-107325310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536726754	chr11:107325357-107325358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548931116	chr11:107325362-107325363	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs199839738	chr11:107325376-107325377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368830590	chr11:107325377-107325378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567448653	chr11:107325466-107325467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544165456	chr11:107325565-107325566	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556386247	chr11:107325581-107325582	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79527219	chr11:107325590-107325591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1981906	chr11:107325616-107325617	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7926690	chr11:107325624-107325625	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs571844676	chr11:107325642-107325643	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542686866	chr11:107325669-107325670	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186286438	chr11:107325703-107325704	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs75477259	chr11:107325742-107325743	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530583	chr11:107325783-107325784	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs148680462	chr11:107325813-107325814	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536386216	chr11:107325821-107325822	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191533685	chr11:107325837-107325838	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565549997	chr11:107325862-107325863	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs35676290	chr11:107325866-107325867	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532564367	chr11:107325879-107325880	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547844171	chr11:107325881-107325882	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Obesity	19966786	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:598 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107241600-107327800	Weak transcription	HSMMtube	muscle
2	chr11:107255000-107327600	Weak transcription	Fetal Heart	heart
3	chr11:107256600-107327600	Weak transcription	NHDF-Ad	bronchial
4	chr11:107269000-107324600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr11:107292800-107327600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr11:107296800-107325600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr11:107297200-107324400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr11:107298200-107327400	Weak transcription	A549	lung
9	chr11:107300400-107326800	Weak transcription	Hela-S3	cervix
10	chr11:107301000-107326800	Weak transcription	HMEC	breast
11	chr11:107307800-107326800	Weak transcription	Fetal Brain Male	brain
12	chr11:107311000-107327400	Weak transcription	Psoas Muscle	Psoas
13	chr11:107313000-107327400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr11:107313400-107327600	Weak transcription	Brain Substantia Nigra	brain
15	chr11:107315400-107326800	Weak transcription	NHEK	skin
16	chr11:107315800-107324800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr11:107317000-107326800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr11:107319000-107325800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr11:107319200-107326600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr11:107319800-107326400	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr11:107320400-107326400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:107320800-107326000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr11:107321600-107325000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr11:107321600-107326400	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr11:107322200-107325200	Strong transcription	GM12878-XiMat	blood
26	chr11:107322200-107326000	Strong transcription	Primary B cells from peripheral blood	blood
27	chr11:107322200-107326400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr11:107322400-107325000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr11:107322400-107325800	Strong transcription	Liver	Liver
30	chr11:107322400-107325800	Strong transcription	Duodenum Smooth Muscle	Duodenum
31	chr11:107322400-107326000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr11:107322600-107324400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr11:107322600-107325000	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr11:107322600-107325000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr11:107322600-107325000	Strong transcription	Stomach Smooth Muscle	stomach
36	chr11:107322600-107325200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr11:107322600-107325200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr11:107322600-107325200	Strong transcription	Adipose Nuclei	Adipose
39	chr11:107322600-107325400	Strong transcription	HUES6 Cell Line	embryonic stem cell
40	chr11:107322600-107325400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
41	chr11:107322600-107325800	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr11:107322800-107325000	Strong transcription	Duodenum Mucosa	Duodenum
43	chr11:107322800-107325000	Strong transcription	Skeletal Muscle Male	skeletal muscle
44	chr11:107322800-107326200	Strong transcription	Dnd41	blood
45	chr11:107323000-107325000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr11:107323000-107325400	Strong transcription	Placenta	Placenta
47	chr11:107323200-107325000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr11:107323200-107325000	Strong transcription	Primary B cells from cord blood	blood
49	chr11:107323200-107325000	Strong transcription	Primary hematopoietic stem cells	blood
50	chr11:107323200-107325000	Strong transcription	Primary hematopoietic stem cells short term culture	blood

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