Variant report

Variant	esv3439101
Chromosome Location	chr11:47657065-47660300
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr11:47648151..47655137-chr11:47656071..47661932,11	K562	blood:
2	chr11:47652437..47655137-chr11:47656639..47658574,2	K562	blood:
3	chr11:47660129..47661788-chr11:47662493..47664105,2	MCF-7	breast:
4	chr11:47655594..47657226-chr11:47658278..47659810,2	K562	blood:
5	chr11:47586161..47588765-chr11:47660200..47662976,2	MCF-7	breast:
6	chr11:47655561..47657543-chr11:47662606..47665556,2	K562	blood:
7	chr11:47655594..47657226-chr11:47658278..47659810,2	K562	blood:
8	chr11:47648507..47652310-chr11:47658295..47660637,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000213619	chromatin interactions
ENSG00000110536	chromatin interactions
ENSG00000149187	chromatin interactions
ENSG00000109919	chromatin interactions

Extended variants
information (count: 139 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:139 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369473982	chr11:47657073-47657074	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs373052204	chr11:47657084-47657085	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs558556021	chr11:47657101-47657102	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565033167	chr11:47657140-47657141	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs530869064	chr11:47657225-47657226	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs193112427	chr11:47657231-47657232	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs560897656	chr11:47657236-47657237	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs79472601	chr11:47657252-47657253	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs77560496	chr11:47657254-47657255	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs545292283	chr11:47657261-47657262	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs199693107	chr11:47657265-47657266	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs546247999	chr11:47657291-47657292	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs566580501	chr11:47657347-47657348	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs35976340	chr11:47657397-47657398	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs147345313	chr11:47657535-47657536	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs552745148	chr11:47657536-47657537	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs569098078	chr11:47657615-47657616	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs538191982	chr11:47657637-47657638	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs554819700	chr11:47657679-47657680	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs139575796	chr11:47657685-47657686	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs534213275	chr11:47657695-47657696	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs34495437	chr11:47657743-47657744	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs553834444	chr11:47657802-47657803	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs553667773	chr11:47657854-47657855	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577278474	chr11:47657860-47657861	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs545972475	chr11:47657910-47657911	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs183629458	chr11:47657937-47657938	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs200118934	chr11:47657944-47657945	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs575490348	chr11:47657975-47657976	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs544554737	chr11:47657994-47657995	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs561185280	chr11:47658005-47658006	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs113364085	chr11:47658006-47658007	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs546575818	chr11:47658071-47658072	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559850780	chr11:47658100-47658101	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs532272380	chr11:47658104-47658105	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs143509249	chr11:47658145-47658146	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs7935802	chr11:47658174-47658175	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs139357300	chr11:47658175-47658176	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs539048751	chr11:47658232-47658233	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs558664426	chr11:47658247-47658248	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs548339819	chr11:47658253-47658254	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs374869462	chr11:47658271-47658272	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs568756923	chr11:47658293-47658294	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs534185772	chr11:47658304-47658305	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs12794570	chr11:47658314-47658315	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs181062448	chr11:47658315-47658316	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs185666211	chr11:47658333-47658334	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs556681309	chr11:47658341-47658342	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs576573994	chr11:47658342-47658343	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs368528350	chr11:47658472-47658473	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:235 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:47636600-47661400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr11:47637600-47657200	Strong transcription	Primary B cells from peripheral blood	blood
3	chr11:47637600-47660800	Strong transcription	Primary neutrophils fromperipheralblood	blood
4	chr11:47637600-47661200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:47637600-47663200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr11:47637800-47660400	Strong transcription	Sigmoid Colon	Sigmoid Colon
7	chr11:47637800-47661000	Strong transcription	Primary T helper cells fromperipheralblood	blood
8	chr11:47637800-47661000	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr11:47638000-47661400	Strong transcription	Fetal Thymus	thymus
10	chr11:47638000-47661800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:47638200-47661200	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr11:47638200-47661200	Strong transcription	Stomach Smooth Muscle	stomach
13	chr11:47638200-47661600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr11:47638200-47661600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr11:47638400-47660400	Strong transcription	Dnd41	blood
16	chr11:47638400-47661200	Strong transcription	HUES6 Cell Line	embryonic stem cell
17	chr11:47638600-47657200	Strong transcription	Skeletal Muscle Female	skeletal muscle
18	chr11:47638800-47661600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr11:47639000-47658000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr11:47639000-47661200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr11:47639000-47661400	Strong transcription	Fetal Muscle Leg	muscle
22	chr11:47639000-47662600	Weak transcription	Stomach Mucosa	stomach
23	chr11:47639200-47657600	Strong transcription	Rectal Mucosa Donor 31	rectum
24	chr11:47639600-47661200	Strong transcription	Fetal Muscle Trunk	muscle
25	chr11:47639800-47657600	Strong transcription	Duodenum Smooth Muscle	Duodenum
26	chr11:47640000-47661000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr11:47640200-47661200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
28	chr11:47640200-47661200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr11:47640200-47661200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr11:47640600-47661400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr11:47640800-47661400	Strong transcription	Fetal Intestine Small	intestine
32	chr11:47640800-47661400	Strong transcription	Fetal Stomach	stomach
33	chr11:47641800-47657600	Strong transcription	Primary T helper cells PMA-I stimulated	--
34	chr11:47641800-47657600	Strong transcription	Cortex derived primary cultured neurospheres	brain
35	chr11:47641800-47659200	Strong transcription	Primary T cells fromperipheralblood	blood
36	chr11:47641800-47661200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr11:47641800-47661600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr11:47642000-47661400	Strong transcription	Placenta	Placenta
39	chr11:47642000-47661800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr11:47643400-47661200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr11:47644000-47661600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr11:47645000-47657200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr11:47646800-47657800	Strong transcription	HUVEC	blood vessel
44	chr11:47646800-47662600	Weak transcription	Aorta	Aorta
45	chr11:47647200-47657200	Strong transcription	NHEK	skin
46	chr11:47648200-47662800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr11:47648200-47663200	Weak transcription	Gastric	stomach
48	chr11:47648400-47662800	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr11:47649200-47662600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr11:47650400-47657200	Strong transcription	iPS-15b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links