Variant report

Variant	nsv896912
Chromosome Location	chr11:4516365-4578530
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:532)
CpG islands
(count:305)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:4560933-4561036	K562	blood:	n/a	n/a
2	ARID3A	chr11:4568278-4568297	HepG2	liver:	n/a	n/a
3	CEBPB	chr11:4540065-4540287	HepG2	liver:	n/a	chr11:4540117-4540130
4	CEBPB	chr11:4516863-4517063	K562	blood:	n/a	n/a
5	CEBPB	chr11:4578528-4578549	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr11:4521600-4521789	H1-hESC	embryonic stem cell:	n/a	chr11:4521689-4521700
7	CEBPB	chr11:4544032-4544147	K562	blood:	n/a	n/a
8	CEBPB	chr11:4569325-4569525	A549	lung:	n/a	chr11:4569397-4569410
9	CEBPB	chr11:4521534-4521859	HepG2	liver:	n/a	chr11:4521689-4521700
10	CEBPB	chr11:4521640-4521844	A549	lung:	n/a	chr11:4521689-4521700
11	CEBPB	chr11:4568337-4568455	HepG2	liver:	n/a	n/a
12	CEBPB	chr11:4521334-4521828	IMR90	lung:	n/a	chr11:4521689-4521700
13	CEBPB	chr11:4551821-4552021	A549	lung:	n/a	n/a
14	CEBPB	chr11:4521549-4521828	K562	blood:	n/a	chr11:4521689-4521700
15	CTCF	chr11:4572960-4573110	AG09309	skin:	n/a	n/a
16	CTCF	chr11:4572908-4573137	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr11:4572920-4573070	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr11:4572946-4573104	ProgFib	skin:	n/a	n/a
19	CTCF	chr11:4560980-4561130	AG10803	skin:	n/a	n/a
20	CTCF	chr11:4560920-4561070	K562	blood:	n/a	n/a
21	CTCF	chr11:4572948-4573099	GM12892	blood:	n/a	n/a
22	CTCF	chr11:4572980-4573130	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr11:4572580-4572730	HCT-116	colon:	n/a	n/a
24	CTCF	chr11:4572960-4573110	HMEC	breast:	n/a	n/a
25	CTCF	chr11:4572640-4573421	A549	lung:	n/a	n/a
26	CTCF	chr11:4560960-4561110	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr11:4572860-4573010	NHDF-neo	bronchial:	n/a	n/a
28	CTCF	chr11:4560848-4561180	HepG2	liver:	n/a	n/a
29	CTCF	chr11:4560960-4561110	HEK293	kidney:	n/a	n/a
30	CTCF	chr11:4572920-4573070	SAEC	small airway:	n/a	n/a
31	CTCF	chr11:4573180-4573330	K562	blood:	n/a	n/a
32	CTCF	chr11:4561000-4561150	HCM	heart:	n/a	n/a
33	CTCF	chr11:4572920-4573070	HFF	foreskin:	n/a	n/a
34	CTCF	chr11:4560882-4561248	MCF-7	breast:	n/a	n/a
35	CTCF	chr11:4560940-4561090	HCT-116	colon:	n/a	n/a
36	CTCF	chr11:4560940-4561090	HepG2	liver:	n/a	n/a
37	CTCF	chr11:4560893-4561186	K562	blood:	n/a	n/a
38	CTCF	chr11:4572900-4573050	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr11:4561000-4561150	HEK293	kidney:	n/a	n/a
40	CTCF	chr11:4560960-4561110	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr11:4561000-4561150	AG09319	gingival:	n/a	n/a
42	CTCF	chr11:4536976-4536979	GM19239	blood:	n/a	n/a
43	CTCF	chr11:4573000-4573150	HCT-116	colon:	n/a	n/a
44	CTCF	chr11:4572949-4573099	MCF-7	breast:	n/a	n/a
45	CTCF	chr11:4560960-4561110	GM12875	blood:	n/a	n/a
46	CTCF	chr11:4560938-4561150	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr11:4560892-4561227	K562	blood:	n/a	n/a
48	CTCF	chr11:4572920-4573070	HPF	lung:	n/a	n/a
49	CTCF	chr11:4560960-4561110	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr11:4572786-4573184	MCF-7	breast:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4566853-4566903	SKMC	muscle:	n/a
2	chr11:4565489-4565539	HL-60	blood:	n/a
3	chr11:4565489-4565539	AG04449	skin:	fetal
4	chr11:4566169-4566219	HepG2	liver:	n/a
5	chr11:4566380-4566430	HEK293	kidney:	embryo
6	chr11:4565489-4565539	U87	brain:	n/a
7	chr11:4566380-4566430	NHDF-neo	bronchial:	n/a
8	chr11:4565475-4565525	Jurkat	blood:	n/a
9	chr11:4566853-4566903	HNPCEpiC	eye:	n/a
10	chr11:4566169-4566219	SKMC	muscle:	n/a
11	chr11:4565475-4565525	HCF	heart:	n/a
12	chr11:4565475-4565525	HIPEpiC	eye:	n/a
13	chr11:4566380-4566430	PFSK-1	brain:	n/a
14	chr11:4565489-4565539	HCF	heart:	n/a
15	chr11:4566169-4566219	HEEpiC	esophagus:	n/a
16	chr11:4566169-4566219	HCT-116	colon:	n/a
17	chr11:4565475-4565525	SK-N-MC	brain:	n/a
18	chr11:4565489-4565539	HRE	kidney:	n/a
19	chr11:4566169-4566219	HAEpiC	amniotic membrane:	n/a
20	chr11:4566853-4566903	AG09309	skin:	n/a
21	chr11:4566853-4566903	HPAEpiC	pulmonary alveolar:	n/a
22	chr11:4566853-4566903	Jurkat	blood:	n/a
23	chr11:4566169-4566219	HPAEpiC	pulmonary alveolar:	n/a
24	chr11:4566380-4566430	PrEC	prostate:	n/a
25	chr11:4566380-4566430	AG09319	gingival:	n/a
26	chr11:4566853-4566903	U87	brain:	n/a
27	chr11:4566380-4566430	HL-60	blood:	n/a
28	chr11:4565489-4565539	SAEC	small airway:	n/a
29	chr11:4565475-4565525	HRE	kidney:	n/a
30	chr11:4566380-4566430	U87	brain:	n/a
31	chr11:4565475-4565525	AG09309	skin:	n/a
32	chr11:4565489-4565539	BJ	skin:	n/a
33	chr11:4565475-4565525	BE2_C	brain:	n/a
34	chr11:4565475-4565525	HCM	heart:	n/a
35	chr11:4565475-4565525	PANC-1	pancreas:	n/a
36	chr11:4566169-4566219	HRPEpiC	eye:	n/a
37	chr11:4566380-4566430	LNCaP	prostate:	n/a
38	chr11:4565489-4565539	NT2-D1	testis:	n/a
39	chr11:4566853-4566903	PrEC	prostate:	n/a
40	chr11:4565475-4565525	NT2-D1	testis:	n/a
41	chr11:4566169-4566219	HEK293	kidney:	embryo
42	chr11:4566380-4566430	GM06990	blood:	n/a
43	chr11:4565475-4565525	GM12891	blood:	n/a
44	chr11:4565489-4565539	ovcar-3	ovarian:	n/a
45	chr11:4566853-4566903	Caco-2	colon:	n/a
46	chr11:4565489-4565539	HUVEC	blood vessel:	n/a
47	chr11:4566853-4566903	HCF	heart:	n/a
48	chr11:4566169-4566219	AG10803	skin:	n/a
49	chr11:4566169-4566219	Hepatocyte	liver:	n/a
50	chr11:4565489-4565539	HPAEpiC	pulmonary alveolar:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:4558523..4560457-chr11:4563023..4565124,2	K562	blood:
2	chr11:4563433..4564999-chr11:4565844..4568054,2	K562	blood:
3	chr11:4208891..4209471-chr11:4572771..4573597,3	MCF-7	breast:
4	chr11:4208014..4209388-chr11:4560615..4561905,12	MCF-7	breast:
5	chr11:4531179..4533009-chr11:4535130..4536667,2	K562	blood:
6	chr11:4535006..4537782-chr11:4538961..4542552,3	K562	blood:
7	chr11:4558523..4560457-chr11:4563023..4565124,2	K562	blood:
8	chr11:4575133..4577035-chr11:4578318..4580954,2	K562	blood:
9	chr11:4531179..4533009-chr11:4535130..4536667,2	K562	blood:
10	chr11:4575133..4577035-chr11:4578318..4580954,2	K562	blood:
11	chr11:4563397..4564933-chr11:4566554..4568624,2	K562	blood:
12	chr11:4563397..4564933-chr11:4566554..4568624,2	K562	blood:
13	chr11:4544362..4546597-chr11:4548286..4550810,3	K562	blood:
14	chr11:4544362..4546597-chr11:4548286..4550810,3	K562	blood:
15	chr11:4208297..4209495-chr11:4560565..4561805,6	K562	blood:
16	chr11:4202964..4204119-chr11:4560777..4561880,3	MCF-7	breast:
17	chr11:4208647..4209327-chr11:4572350..4573087,2	MCF-7	breast:
18	chr11:4208191..4209065-chr11:4560550..4561852,3	MCF-7	breast:

No data

Variant related genes	Relation type
OR52M1	TF binding region
OR52M2P	TF binding region
OR52M1	CpG island
OR52M2P	CpG island
ENSG00000226616	chromatin interactions
ENSG00000197790	chromatin interactions
ENSG00000254480	chromatin interactions

Extended variants
information (count: 2304 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2304 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10160717	chr11:4516365-4516366	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188066560	chr11:4516369-4516370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs331516	chr11:4516382-4516383	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs547145266	chr11:4516402-4516403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556115309	chr11:4516410-4516411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562448159	chr11:4516419-4516420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs577379869	chr11:4516421-4516422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73427711	chr11:4516451-4516452	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs141345399	chr11:4516470-4516471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559964193	chr11:4516491-4516492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528556628	chr11:4516509-4516510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552769865	chr11:4516519-4516520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540757325	chr11:4516538-4516539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10160399	chr11:4516576-4516577	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
15	rs529310225	chr11:4516621-4516622	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs145190004	chr11:4516648-4516649	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs139005012	chr11:4516694-4516695	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs192585833	chr11:4516707-4516708	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs386750003	chr11:4516708-4516709	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs116725533	chr11:4516709-4516710	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs114162456	chr11:4516713-4516714	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs555458425	chr11:4516769-4516770	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs567101791	chr11:4516773-4516774	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs370006921	chr11:4516775-4516776	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs555783196	chr11:4516782-4516783	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs141987359	chr11:4516809-4516810	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs150407352	chr11:4516832-4516833	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs184230434	chr11:4516833-4516834	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs572221350	chr11:4516843-4516844	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs550033950	chr11:4516862-4516863	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs368725137	chr11:4516890-4516891	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs73427713	chr11:4516892-4516893	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs138126059	chr11:4516902-4516903	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs577166522	chr11:4516910-4516911	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs574547103	chr11:4516912-4516913	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs528978441	chr11:4516917-4516918	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs544613816	chr11:4516926-4516927	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs369573697	chr11:4516950-4516951	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs569880632	chr11:4516978-4516979	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs149588940	chr11:4516985-4516986	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs528738462	chr11:4516996-4516997	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs552117371	chr11:4517004-4517005	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs567040064	chr11:4517013-4517014	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs527887351	chr11:4517017-4517018	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs548765389	chr11:4517025-4517026	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs567348460	chr11:4517041-4517042	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs576560863	chr11:4517060-4517061	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs537591606	chr11:4517065-4517066	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs12292161	chr11:4517128-4517129	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs184543	chr11:4517132-4517133	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	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
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Bipolar disorder	19114987	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	23613489	CNVD

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4514400-4516400	Weak transcription	Fetal Heart	heart
2	chr11:4514600-4517000	Weak transcription	Placenta	Placenta
3	chr11:4514600-4517400	Weak transcription	Ovary	ovary
4	chr11:4514600-4517800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr11:4514600-4518000	Weak transcription	Liver	Liver
6	chr11:4516400-4518800	Enhancers	Fetal Heart	heart
7	chr11:4516600-4517600	Bivalent Enhancer	Fetal Lung	lung
8	chr11:4517000-4519000	Enhancers	Placenta	Placenta
9	chr11:4517400-4517600	Enhancers	Ovary	ovary
10	chr11:4517600-4517800	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr11:4517600-4517800	Flanking Bivalent TSS/Enh	Fetal Lung	lung
12	chr11:4517600-4517800	Flanking Active TSS	Ovary	ovary
13	chr11:4517600-4518000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
14	chr11:4517600-4518000	Enhancers	Stomach Smooth Muscle	stomach
15	chr11:4517600-4518400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr11:4517600-4518800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr11:4517600-4518800	Bivalent Enhancer	NHEK	skin
18	chr11:4517800-4518000	Bivalent/Poised TSS	Fetal Lung	lung
19	chr11:4517800-4518200	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr11:4517800-4518200	Enhancers	Brain Anterior Caudate	brain
21	chr11:4517800-4518200	Enhancers	Fetal Brain Female	brain
22	chr11:4517800-4518200	Active TSS	Ovary	ovary
23	chr11:4517800-4518400	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr11:4518000-4518200	Flanking Bivalent TSS/Enh	Fetal Lung	lung
25	chr11:4518000-4518200	Flanking Active TSS	Stomach Smooth Muscle	stomach
26	chr11:4518000-4518200	Bivalent Enhancer	NHDF-Ad	bronchial
27	chr11:4518000-4518400	Enhancers	Liver	Liver
28	chr11:4518000-4518600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr11:4518200-4518400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr11:4518200-4518600	Bivalent Enhancer	Fetal Lung	lung
31	chr11:4518200-4519200	Enhancers	Ovary	ovary
32	chr11:4524200-4524400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr11:4524400-4525400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr11:4529800-4530800	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr11:4530000-4530400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr11:4530200-4530600	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr11:4530800-4533000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr11:4531000-4531200	Enhancers	Colon Smooth Muscle	Colon
39	chr11:4531200-4531400	Enhancers	Stomach Smooth Muscle	stomach
40	chr11:4531400-4532600	Weak transcription	Colon Smooth Muscle	Colon
41	chr11:4531400-4532800	Weak transcription	Stomach Smooth Muscle	stomach
42	chr11:4531800-4534200	Enhancers	Ovary	ovary
43	chr11:4532000-4534000	Enhancers	Fetal Lung	lung
44	chr11:4532200-4533000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr11:4532400-4532800	Enhancers	Gastric	stomach
46	chr11:4532400-4533000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr11:4532600-4533600	Enhancers	Rectal Smooth Muscle	rectum
48	chr11:4532600-4535600	Enhancers	Colon Smooth Muscle	Colon
49	chr11:4532800-4533000	Enhancers	Stomach Smooth Muscle	stomach
50	chr11:4533000-4534000	Weak transcription	Stomach Smooth Muscle	stomach

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