Variant report

Variant	nsv467714
Chromosome Location	chr11:17513147-17521825
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:188)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:188 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr11:17519723-17520008	HepG2	liver:	n/a	n/a
2	CEBPB	chr11:17519549-17520016	MCF-7	breast:	n/a	n/a
3	CEBPB	chr11:17519671-17519920	A549	lung:	n/a	n/a
4	CEBPB	chr11:17519669-17519957	HepG2	liver:	n/a	n/a
5	CEBPB	chr11:17519582-17520194	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr11:17519686-17519980	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr11:17519630-17519990	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr11:17520140-17520290	GM06990	blood:	n/a	n/a
9	CTCF	chr11:17520140-17520290	HCFaa	heart:	n/a	n/a
10	CTCF	chr11:17520080-17520230	HepG2	liver:	n/a	n/a
11	CTCF	chr11:17520100-17520250	GM12872	blood:	n/a	n/a
12	CTCF	chr11:17515700-17515850	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr11:17520032-17520319	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr11:17520140-17520290	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr11:17520780-17520930	HepG2	liver:	n/a	n/a
16	CTCF	chr11:17520060-17520210	HRE	kidney:	n/a	n/a
17	CTCF	chr11:17520120-17520270	HVMF	connective:	n/a	n/a
18	CTCF	chr11:17520120-17520270	HPF	lung:	n/a	n/a
19	CTCF	chr11:17520200-17520350	AG10803	skin:	n/a	n/a
20	CTCF	chr11:17520180-17520330	GM12872	blood:	n/a	n/a
21	CTCF	chr11:17519784-17519858	ProgFib	skin:	n/a	n/a
22	CTCF	chr11:17520140-17520276	ProgFib	skin:	n/a	n/a
23	CTCF	chr11:17519725-17519908	MCF-7	breast:	n/a	n/a
24	CTCF	chr11:17520120-17520370	NHLF	lung:	n/a	n/a
25	CTCF	chr11:17520160-17520310	AG04450	lung:	n/a	n/a
26	CTCF	chr11:17520160-17520310	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr11:17520143-17520258	MCF-7	breast:	n/a	n/a
28	CTCF	chr11:17520100-17520250	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr11:17514880-17515030	WERI-Rb-1	eye:	n/a	chr11:17514953-17514962
30	CTCF	chr11:17519640-17519790	HEK293	kidney:	n/a	n/a
31	CTCF	chr11:17520027-17520381	GM12878	blood:	n/a	n/a
32	CTCF	chr11:17520100-17520250	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr11:17520120-17520270	BJ	skin:	n/a	n/a
34	CTCF	chr11:17520200-17520350	SAEC	small airway:	n/a	n/a
35	CTCF	chr11:17520137-17520248	MCF-7	breast:	n/a	n/a
36	CTCF	chr11:17520120-17520270	AG10803	skin:	n/a	n/a
37	CTCF	chr11:17520060-17520210	HAc	cerebellar:	n/a	n/a
38	CTCF	chr11:17520120-17520270	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr11:17520120-17520270	AG04449	skin:	n/a	n/a
40	CTCF	chr11:17520123-17520322	K562	blood:	n/a	n/a
41	CTCF	chr11:17520160-17520310	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr11:17520120-17520270	NHEK	skin:	n/a	n/a
43	CTCF	chr11:17520120-17520270	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr11:17520140-17520290	MCF-7	breast:	n/a	n/a
45	CTCF	chr11:17520120-17520270	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr11:17520140-17520290	GM12868	blood:	n/a	n/a
47	CTCF	chr11:17520136-17520288	GM13977	blood:	n/a	n/a
48	CTCF	chr11:17520140-17520290	GM12878	blood:	n/a	n/a
49	CTCF	chr11:17520140-17520290	GM12874	blood:	n/a	n/a
50	CTCF	chr11:17520120-17520270	HPAF	blood vessel:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17520223-17520273	ovcar-3	ovarian:	n/a
2	chr11:17515836-17515886	PFSK-1	brain:	n/a
3	chr11:17520223-17520273	AG04450	lung:	fetal
4	chr11:17520223-17520273	HAEpiC	amniotic membrane:	n/a
5	chr11:17515836-17515886	Caco-2	colon:	n/a
6	chr11:17515836-17515886	HRE	kidney:	n/a
7	chr11:17515836-17515886	ECC-1	luminal epithelium:	n/a
8	chr11:17515836-17515886	Jurkat	blood:	n/a
9	chr11:17515836-17515886	AG09309	skin:	n/a
10	chr11:17520223-17520273	HEK293	kidney:	embryo
11	chr11:17520223-17520273	H1-hESC	embryonic stem cell:	embryo
12	chr11:17515836-17515886	GM12878	blood:	n/a
13	chr11:17515836-17515886	GM19239	blood:	n/a
14	chr11:17515836-17515886	HCM	heart:	n/a
15	chr11:17520223-17520273	GM12878	blood:	n/a
16	chr11:17520223-17520273	AG04449	skin:	fetal
17	chr11:17520223-17520273	NHDF-neo	bronchial:	n/a
18	chr11:17515836-17515886	HAEpiC	amniotic membrane:	n/a
19	chr11:17520223-17520273	PANC-1	pancreas:	n/a
20	chr11:17520223-17520273	HNPCEpiC	eye:	n/a
21	chr11:17520223-17520273	AoSMC	blood vessel:	n/a
22	chr11:17520223-17520273	SK-N-MC	brain:	n/a
23	chr11:17515836-17515886	IMR90	lung:	fetal
24	chr11:17515836-17515886	HUVEC	blood vessel:	n/a
25	chr11:17515836-17515886	PANC-1	pancreas:	n/a
26	chr11:17515836-17515886	SK-N-MC	brain:	n/a
27	chr11:17520223-17520273	AG10803	skin:	n/a
28	chr11:17520223-17520273	HCM	heart:	n/a
29	chr11:17520223-17520273	SKMC	muscle:	n/a
30	chr11:17520223-17520273	HCF	heart:	n/a
31	chr11:17520223-17520273	MCF-7	breast:	n/a
32	chr11:17520223-17520273	BE2_C	brain:	n/a
33	chr11:17515836-17515886	HCF	heart:	n/a
34	chr11:17515836-17515886	HPAEpiC	pulmonary alveolar:	n/a
35	chr11:17520223-17520273	GM19239	blood:	n/a
36	chr11:17520223-17520273	Jurkat	blood:	n/a
37	chr11:17520223-17520273	HUVEC	blood vessel:	n/a
38	chr11:17520223-17520273	PFSK-1	brain:	n/a
39	chr11:17515836-17515886	GM12892	blood:	n/a
40	chr11:17515836-17515886	HNPCEpiC	eye:	n/a
41	chr11:17515836-17515886	NH-A	brain:	n/a
42	chr11:17515836-17515886	BJ	skin:	n/a
43	chr11:17515836-17515886	GM06990	blood:	n/a
44	chr11:17515836-17515886	AoSMC	blood vessel:	n/a
45	chr11:17515836-17515886	MCF10A-Er-Src	breast:	n/a
46	chr11:17520223-17520273	SK-N-SH	brain:	n/a
47	chr11:17515836-17515886	RPTEC	kidney:	n/a
48	chr11:17520223-17520273	HIPEpiC	eye:	n/a
49	chr11:17520223-17520273	ECC-1	luminal epithelium:	n/a
50	chr11:17515836-17515886	SKMC	muscle:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:17520408..17522288-chr11:17583277..17586222,2	K562	blood:
2	chr11:17094293..17097227-chr11:17519286..17521617,2	K562	blood:
3	chr11:17232194..17233796-chr11:17514149..17515893,2	MCF-7	breast:
4	chr11:17405333..17406124-chr11:17519578..17520279,2	MCF-7	breast:
5	chr11:17514979..17516767-chr11:17519938..17522718,2	K562	blood:
6	chr11:17410518..17411123-chr11:17519560..17520298,2	MCF-7	breast:
7	chr11:17513527..17517514-chr11:17518816..17522718,5	K562	blood:
8	chr11:17514979..17516767-chr11:17519938..17522718,2	K562	blood:
9	chr11:17513527..17517514-chr11:17518816..17522718,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCC8-2	chr11:17515447-17516640	NONHSAT018237

No data

Variant related genes	Relation type
USH1C	TF binding region
USH1C	CpG island
ENSG00000221322	chromatin interactions
ENSG00000187486	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000272034	chromatin interactions

Extended variants
information (count: 395 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17703233	chr11:17513147-17513148	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565569844	chr11:17513154-17513155	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs532637276	chr11:17513206-17513207	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs551138619	chr11:17513219-17513220	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs146806423	chr11:17513224-17513225	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs547800613	chr11:17513263-17513264	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs566092514	chr11:17513271-17513272	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs140622425	chr11:17513278-17513279	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs535476814	chr11:17513350-17513351	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs6486374	chr11:17513389-17513390	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs56170308	chr11:17513407-17513408	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs556296301	chr11:17513423-17513424	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs6486375	chr11:17513426-17513427	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs6486376	chr11:17513446-17513447	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs113997306	chr11:17513452-17513453	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs145613390	chr11:17513475-17513476	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs540622991	chr11:17513511-17513512	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs559021820	chr11:17513530-17513531	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs577447642	chr11:17513558-17513559	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs6486377	chr11:17513563-17513564	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs563066216	chr11:17513600-17513601	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138152519	chr11:17513606-17513607	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541570333	chr11:17513634-17513635	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs202031224	chr11:17513676-17513677	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527319899	chr11:17513677-17513678	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552127092	chr11:17513772-17513773	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536848882	chr11:17513797-17513798	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187355935	chr11:17513800-17513801	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs4757533	chr11:17513815-17513816	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs549717127	chr11:17513827-17513828	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs568212738	chr11:17513836-17513837	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs535643702	chr11:17513878-17513879	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553126987	chr11:17513884-17513885	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs575879316	chr11:17513889-17513890	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs12576915	chr11:17513943-17513944	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs541050971	chr11:17514066-17514067	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs566954697	chr11:17514120-17514121	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533968169	chr11:17514155-17514156	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143416621	chr11:17514189-17514190	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs559279502	chr11:17514190-17514191	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556485978	chr11:17514215-17514216	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148344738	chr11:17514237-17514238	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs4756895	chr11:17514252-17514253	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs527409985	chr11:17514255-17514256	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559841166	chr11:17514294-17514295	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs917276	chr11:17514301-17514302	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs4756896	chr11:17514347-17514348	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs917277	chr11:17514365-17514366	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs4756897	chr11:17514392-17514393	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs377583924	chr11:17514417-17514418	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
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
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Usher syndrome	20538994	CNVD
Usher type I cohort	21436283	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17507800-17515800	Weak transcription	Gastric	stomach
2	chr11:17508800-17515600	Weak transcription	Fetal Intestine Large	intestine
3	chr11:17510600-17513200	Bivalent Enhancer	Fetal Muscle Leg	muscle
4	chr11:17511200-17526000	Weak transcription	Brain Substantia Nigra	brain
5	chr11:17511800-17513200	Enhancers	Adipose Nuclei	Adipose
6	chr11:17512400-17515200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr11:17512600-17513400	Enhancers	Fetal Intestine Small	intestine
8	chr11:17512600-17530000	Weak transcription	Right Atrium	heart
9	chr11:17513400-17513600	Weak transcription	Fetal Intestine Small	intestine
10	chr11:17513400-17515200	Bivalent Enhancer	Fetal Muscle Leg	muscle
11	chr11:17513600-17514200	Enhancers	Right Ventricle	heart
12	chr11:17513600-17514800	Enhancers	Pancreas	Pancrea
13	chr11:17513600-17530600	Strong transcription	Fetal Intestine Small	intestine
14	chr11:17514000-17514200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
15	chr11:17514200-17515000	Bivalent Enhancer	Placenta	Placenta
16	chr11:17514200-17515000	Enhancers	Dnd41	blood
17	chr11:17514200-17516000	Weak transcription	Duodenum Mucosa	Duodenum
18	chr11:17514400-17514800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr11:17514800-17515000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr11:17514800-17522800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr11:17515000-17516200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
22	chr11:17515000-17523600	Weak transcription	Dnd41	blood
23	chr11:17515200-17515600	Enhancers	Fetal Muscle Leg	muscle
24	chr11:17515400-17517800	Weak transcription	Colonic Mucosa	Colon
25	chr11:17515600-17524600	Strong transcription	Fetal Intestine Large	intestine
26	chr11:17515800-17516000	Enhancers	Gastric	stomach
27	chr11:17515800-17518600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr11:17516000-17518000	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr11:17516000-17519600	Weak transcription	Gastric	stomach
30	chr11:17516000-17523000	Strong transcription	Duodenum Mucosa	Duodenum
31	chr11:17516400-17516600	Enhancers	Fetal Muscle Leg	muscle
32	chr11:17516600-17517800	Weak transcription	Fetal Muscle Leg	muscle
33	chr11:17516800-17529600	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr11:17516800-17553000	Weak transcription	Stomach Mucosa	stomach
35	chr11:17517200-17519000	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr11:17517600-17518400	Enhancers	Adipose Nuclei	Adipose
37	chr11:17517800-17518000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr11:17517800-17518400	Enhancers	Fetal Muscle Leg	muscle
39	chr11:17517800-17519000	Strong transcription	Colonic Mucosa	Colon
40	chr11:17518000-17518400	Enhancers	Brain Germinal Matrix	brain
41	chr11:17518000-17522800	Strong transcription	Rectal Mucosa Donor 31	rectum
42	chr11:17518400-17519600	Weak transcription	Brain Germinal Matrix	brain
43	chr11:17519000-17521200	Weak transcription	Colonic Mucosa	Colon
44	chr11:17519000-17521800	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr11:17519400-17520200	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr11:17519600-17520000	Enhancers	Gastric	stomach
47	chr11:17519600-17520200	Enhancers	H1 Cell Line	embryonic stem cell
48	chr11:17519800-17520000	Enhancers	Brain Germinal Matrix	brain
49	chr11:17519800-17520000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
50	chr11:17519800-17520200	Enhancers	Esophagus	oesophagus

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