Variant report

Variant	nsv898328
Chromosome Location	chr11:100993846-101009933
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:220)
CpG islands
(count:1099)
Chromatin interactive
region (count:30)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:220 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr11:100997677-100997877	K562	blood:	n/a	n/a
2	BHLHE40	chr11:100998753-100999278	K562	blood:	n/a	n/a
3	CCNT2	chr11:100997898-100999157	K562	blood:	n/a	chr11:100998077-100998086
4	CCNT2	chr11:100999671-100999884	K562	blood:	n/a	n/a
5	CEBPB	chr11:100994723-100994987	K562	blood:	n/a	n/a
6	CEBPB	chr11:101001835-101002083	HepG2	liver:	n/a	chr11:101001959-101001970
7	CEBPB	chr11:101001874-101002105	K562	blood:	n/a	chr11:101001959-101001970
8	CHD2	chr11:100998735-100998746	K562	blood:	n/a	n/a
9	CTBP2	chr11:100997627-100999305	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTBP2	chr11:100999654-101000641	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr11:100998798-100999274	K562	blood:	n/a	n/a
12	CTCF	chr11:100998840-100998990	WERI-Rb-1	eye:	n/a	n/a
13	CTCF	chr11:100998827-100998948	Pancreas_OC	pancreas:	n/a	n/a
14	CTCF	chr11:100998940-100999090	AG09319	gingival:	n/a	n/a
15	CTCF	chr11:100998894-100999168	K562	blood:	n/a	n/a
16	CTCF	chr11:100998848-100998987	A549	lung:	n/a	n/a
17	CTCF	chr11:101007143-101007175	LNCaP	prostate:	n/a	n/a
18	CTCF	chr11:100998800-100998950	Caco-2	colon:	n/a	n/a
19	CTCF	chr11:100999067-100999072	MCF-7	breast:	n/a	n/a
20	CTCF	chr11:100998870-100998926	NHEK	skin:	n/a	n/a
21	CTCF	chr11:100998853-100998949	MCF-7	breast:	n/a	n/a
22	CTCF	chr11:100999961-100999986	MCF-7	breast:	n/a	n/a
23	CTCF	chr11:100998860-100999010	HEK293	kidney:	n/a	n/a
24	CTCF	chr11:100998864-100999074	K562	blood:	n/a	n/a
25	CTCF	chr11:100998845-100999029	MCF-7	breast:	n/a	n/a
26	CTCF	chr11:100998838-100999065	MCF-7	breast:	n/a	n/a
27	CTCF	chr11:100998940-100999090	AG04449	skin:	n/a	n/a
28	CTCF	chr11:100998865-100999055	MCF-7	breast:	n/a	n/a
29	CTCF	chr11:100998861-100998989	MCF-7	breast:	n/a	n/a
30	CTCF	chr11:100999860-101000010	K562	blood:	n/a	n/a
31	CTCF	chr11:100999934-101000004	MCF-7	breast:	n/a	n/a
32	E2F4	chr11:101002761-101002924	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr11:101003829-101004266	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F6	chr11:100998330-100999388	H1-hESC	embryonic stem cell:	n/a	n/a
35	E2F6	chr11:101000072-101000321	K562	blood:	n/a	n/a
36	E2F6	chr11:100998229-100999107	K562	blood:	n/a	n/a
37	E2F6	chr11:100998870-100999011	K562	blood:	n/a	n/a
38	E2F6	chr11:100998013-100999182	H1-hESC	embryonic stem cell:	n/a	chr11:100998100-100998110
39	E2F6	chr11:100999611-100999859	K562	blood:	n/a	n/a
40	E2F6	chr11:100998019-101000444	K562	blood:	n/a	chr11:100999948-100999957 chr11:100999948-100999960 chr11:100998100-100998110
41	EGR1	chr11:101000320-101000735	K562	blood:	n/a	n/a
42	EGR1	chr11:100999800-101000054	K562	blood:	n/a	chr11:100999949-100999962 chr11:100999948-100999958 chr11:100999943-100999956
43	EGR1	chr11:100998115-100998637	K562	blood:	n/a	n/a
44	EGR1	chr11:100998157-100998396	K562	blood:	n/a	n/a
45	EGR1	chr11:100998882-100999152	K562	blood:	n/a	n/a
46	EGR1	chr11:100998435-100998637	K562	blood:	n/a	n/a
47	EGR1	chr11:101000258-101000689	MCF-7	breast:	n/a	chr11:101000286-101000301 chr11:101000287-101000300
48	EGR1	chr11:101000363-101000630	K562	blood:	n/a	n/a
49	EGR1	chr11:101003828-101004419	HCT-116	colon:	n/a	n/a
50	EGR1	chr11:100998876-100999137	K562	blood:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:100999399-100999449	PANC-1	pancreas:	n/a
2	chr11:100999399-100999449	PANC-1	pancreas:	n/a
3	chr11:101001711-101001761	PANC-1	pancreas:	n/a
4	chr11:101001711-101001761	SAEC	small airway:	n/a
5	chr11:101002821-101002871	NHDF-neo	bronchial:	n/a
6	chr11:100999009-100999059	GM12878	blood:	n/a
7	chr11:100999077-100999127	SAEC	small airway:	n/a
8	chr11:100997799-100997849	NB4	blood:	n/a
9	chr11:101000164-101000214	SKMC	muscle:	n/a
10	chr11:101000436-101000486	NB4	blood:	n/a
11	chr11:100999009-100999059	HCPEpiC	choroid plexus:	n/a
12	chr11:100997799-100997849	GM12878	blood:	n/a
13	chr11:101000618-101000668	HL-60	blood:	n/a
14	chr11:100998943-100998993	AG09319	gingival:	n/a
15	chr11:101000566-101000616	H1-hESC	embryonic stem cell:	embryo
16	chr11:101000717-101000767	ECC-1	luminal epithelium:	n/a
17	chr11:101000717-101000767	SK-N-SH_RA	brain:	n/a
18	chr11:101000436-101000486	PFSK-1	brain:	n/a
19	chr11:101001257-101001307	HIPEpiC	eye:	n/a
20	chr11:101000436-101000486	LNCaP	prostate:	n/a
21	chr11:100997799-100997849	LNCaP	prostate:	n/a
22	chr11:101000436-101000486	ECC-1	luminal epithelium:	n/a
23	chr11:100999399-100999449	SKMC	muscle:	n/a
24	chr11:100999077-100999127	HCM	heart:	n/a
25	chr11:100997799-100997849	PFSK-1	brain:	n/a
26	chr11:100997799-100997849	HRPEpiC	eye:	n/a
27	chr11:100999953-101000003	LNCaP	prostate:	n/a
28	chr11:100999077-100999127	GM19239	blood:	n/a
29	chr11:100999009-100999059	HRCEpiC	kidney:	n/a
30	chr11:101002821-101002871	MCF-7	breast:	n/a
31	chr11:101000717-101000767	HNPCEpiC	eye:	n/a
32	chr11:101000618-101000668	AG09309	skin:	n/a
33	chr11:101000589-101000639	BE2_C	brain:	n/a
34	chr11:101000164-101000214	HUVEC	blood vessel:	n/a
35	chr11:101000164-101000214	GM12878	blood:	n/a
36	chr11:100994089-100994139	ovcar-3	ovarian:	n/a
37	chr11:101000655-101000705	HIPEpiC	eye:	n/a
38	chr11:100999953-101000003	SAEC	small airway:	n/a
39	chr11:101000655-101000705	HRE	kidney:	n/a
40	chr11:101000717-101000767	HEEpiC	esophagus:	n/a
41	chr11:101001257-101001307	GM12892	blood:	n/a
42	chr11:101000589-101000639	AG09309	skin:	n/a
43	chr11:101001711-101001761	T-47D	breast:	n/a
44	chr11:100999953-101000003	HIPEpiC	eye:	n/a
45	chr11:100999077-100999127	MCF-7	breast:	n/a
46	chr11:100999399-100999449	PrEC	prostate:	n/a
47	chr11:100999077-100999127	BE2_C	brain:	n/a
48	chr11:100999399-100999449	HCT-116	colon:	n/a
49	chr11:101000566-101000616	PFSK-1	brain:	n/a
50	chr11:101000589-101000639	HCM	heart:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:100997015..100999242-chr11:101300083..101302474,2	MCF-7	breast:
2	chr11:100994873..100997835-chr11:101312314..101314341,3	MCF-7	breast:
3	chr11:100905153..100907008-chr11:100991941..100994104,2	MCF-7	breast:
4	chr11:100992998..100996575-chr11:101047325..101050411,3	MCF-7	breast:
5	chr11:100997196..100999352-chr11:101219935..101222787,2	MCF-7	breast:
6	chr11:100820823..100823466-chr11:100993922..100996465,2	K562	blood:
7	chr11:100996775..100999414-chr11:101040278..101042941,3	MCF-7	breast:
8	chr11:100995755..100998186-chr17:61027837..61029575,2	MCF-7	breast:
9	chr11:100997510..100999276-chr11:101077544..101080289,2	MCF-7	breast:
10	chr11:100993173..100995735-chr11:101190214..101191765,2	MCF-7	breast:
11	chr11:100997950..100999651-chr11:101197164..101199921,2	MCF-7	breast:
12	chr11:100985987..100991412-chr11:100992377..100996760,6	K562	blood:
13	chr11:100947424..100949446-chr11:100997091..100999077,2	MCF-7	breast:
14	chr11:101004314..101006234-chr11:101008829..101011462,2	K562	blood:
15	chr11:100989846..100992410-chr11:100997407..100999577,3	K562	blood:
16	chr11:100961948..100963629-chr11:100991908..100994772,2	MCF-7	breast:
17	chr11:100851290..100854016-chr11:100995188..100997674,2	MCF-7	breast:
18	chr11:100994260..100996186-chr11:101205184..101207862,2	MCF-7	breast:
19	chr11:100998097..100998597-chr4:78741144..78741880,2	Hela-S3	cervix:
20	chr11:100992960..100995001-chr11:101041682..101044528,2	MCF-7	breast:
21	chr11:100988771..100991536-chr11:100994068..100996057,2	K562	blood:
22	chr11:100953156..100955270-chr11:100996509..100998823,2	MCF-7	breast:
23	chr11:100817953..100820202-chr11:100996592..100999547,2	MCF-7	breast:
24	chr11:100862479..100864275-chr11:100997401..100999595,2	MCF-7	breast:
25	chr11:100906950..100909158-chr11:100997718..100999682,2	MCF-7	breast:
26	chr11:100984450..100986549-chr11:100993065..100996341,3	MCF-7	breast:
27	chr11:101004314..101006234-chr11:101008829..101011462,2	K562	blood:
28	chr11:100933625..100935266-chr11:100997720..101000555,2	MCF-7	breast:
29	chr1:193681603..193683732-chr11:100996114..100998464,2	MCF-7	breast:
30	chr11:100964171..100966264-chr11:100996751..100998539,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM133-3	chr11:100999808-101000619	NONHSAT023850
2	lnc-TMEM133-3	chr11:101003742-101003856	NONHSAT023851
3	lnc-TMEM133-3	chr11:101003742-101003856	NONHSAT023850
4	lnc-TMEM133-3	chr11:100999808-101000619	NONHSAT023851
5	lnc-TMEM133-3	chr11:101001420-101001513	NONHSAT023851
6	lnc-TMEM133-3	chr11:101001420-101001513	NONHSAT023850

No data

Variant related genes	Relation type
PGR	TF binding region
PGR	CpG island
ENSG00000255504	chromatin interactions
ENSG00000170647	chromatin interactions
ENSG00000082175	chromatin interactions
ENSG00000265262	chromatin interactions

Extended variants
information (count: 620 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:620 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529359	chr11:100993846-100993847	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576112069	chr11:100993902-100993903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189218972	chr11:100993924-100993925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544050938	chr11:100993956-100993957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs118124681	chr11:100993984-100993985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529713662	chr11:100994002-100994003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs35370108	chr11:100994070-100994071	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs560335468	chr11:100994072-100994073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532134812	chr11:100994090-100994091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552236186	chr11:100994102-100994103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs74551360	chr11:100994112-100994113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557256629	chr11:100994121-100994122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575414388	chr11:100994122-100994123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192505204	chr11:100994138-100994139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182395405	chr11:100994142-100994143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568643376	chr11:100994194-100994195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs34485330	chr11:100994204-100994205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534171182	chr11:100994223-100994224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553841395	chr11:100994282-100994283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs576959946	chr11:100994290-100994291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs186725606	chr11:100994362-100994363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556545798	chr11:100994365-100994366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138732328	chr11:100994369-100994370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564601846	chr11:100994415-100994416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117112396	chr11:100994420-100994421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559605894	chr11:100994446-100994447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs34350624	chr11:100994458-100994459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191283063	chr11:100994467-100994468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542888111	chr11:100994472-100994473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374318142	chr11:100994523-100994524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540472437	chr11:100994568-100994569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571827530	chr11:100994619-100994620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374700872	chr11:100994626-100994627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs481775	chr11:100994675-100994676	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs34445416	chr11:100994749-100994750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs34762352	chr11:100994823-100994824	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562513574	chr11:100994834-100994835	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs144843450	chr11:100994839-100994840	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs35595684	chr11:100994845-100994846	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs35416901	chr11:100994849-100994850	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs582691	chr11:100994866-100994867	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs580512	chr11:100994882-100994883	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs570586629	chr11:100994899-100994900	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs148177226	chr11:100994940-100994941	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564011901	chr11:100994988-100994989	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs377219616	chr11:100995019-100995020	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs484682	chr11:100995021-100995022	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs564143137	chr11:100995040-100995041	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs535525279	chr11:100995133-100995134	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142936731	chr11:100995139-100995140	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Melanoma	22183965	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal cancer	21851588	CNVD
Multiple myeloma	17550852	CNVD

Chromatin state (count:410 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:100905400-100997600	Weak transcription	Left Ventricle	heart
2	chr11:100975800-100996800	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr11:100978000-100996400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr11:100983400-100994800	Weak transcription	Aorta	Aorta
5	chr11:100985800-100994000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr11:100991000-100997200	Weak transcription	Right Ventricle	heart
7	chr11:100993600-100994200	Enhancers	Ovary	ovary
8	chr11:100994000-100995800	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr11:100994000-100996600	Weak transcription	K562	blood
10	chr11:100994200-100994800	Weak transcription	Ovary	ovary
11	chr11:100994800-100995800	Active TSS	Aorta	Aorta
12	chr11:100994800-100995800	Active TSS	Ovary	ovary
13	chr11:100995000-100995600	Enhancers	Colon Smooth Muscle	Colon
14	chr11:100995600-100996800	Weak transcription	Colon Smooth Muscle	Colon
15	chr11:100995800-100996000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr11:100995800-100996600	Weak transcription	Aorta	Aorta
17	chr11:100995800-100996600	Weak transcription	Ovary	ovary
18	chr11:100996000-100996400	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr11:100996400-100996600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr11:100996400-100996800	Bivalent Enhancer	Fetal Lung	lung
21	chr11:100996400-100999400	Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr11:100996600-100997200	Enhancers	Adipose Nuclei	Adipose
23	chr11:100996600-100999400	Active TSS	Right Atrium	heart
24	chr11:100996600-101000600	Active TSS	Aorta	Aorta
25	chr11:100996600-101000600	Active TSS	K562	blood
26	chr11:100996600-101000800	Active TSS	Ovary	ovary
27	chr11:100996600-101001200	Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr11:100996800-100997000	Flanking Bivalent TSS/Enh	Fetal Lung	lung
29	chr11:100996800-100997200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
30	chr11:100996800-100997400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr11:100996800-100997600	Active TSS	Duodenum Smooth Muscle	Duodenum
32	chr11:100996800-100998800	Active TSS	Rectal Smooth Muscle	rectum
33	chr11:100996800-101000800	Active TSS	Colon Smooth Muscle	Colon
34	chr11:100997000-100997200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
35	chr11:100997000-100997200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
36	chr11:100997000-100997800	Active TSS	Stomach Smooth Muscle	stomach
37	chr11:100997000-100999800	Bivalent/Poised TSS	Fetal Lung	lung
38	chr11:100997200-100997400	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
39	chr11:100997200-100997400	Active TSS	Adipose Nuclei	Adipose
40	chr11:100997200-100997400	Bivalent/Poised TSS	Liver	Liver
41	chr11:100997200-100997600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
42	chr11:100997200-100997600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
43	chr11:100997200-100997600	Bivalent Enhancer	Fetal Kidney	kidney
44	chr11:100997200-100997600	Active TSS	Skeletal Muscle Female	skeletal muscle
45	chr11:100997200-100999200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr11:100997200-100999200	Active TSS	Right Ventricle	heart
47	chr11:100997200-100999400	Active TSS	NHDF-Ad	bronchial
48	chr11:100997200-101000600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
49	chr11:100997200-101000600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
50	chr11:100997400-100997600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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