Variant report

Variant	esv2762895
Chromosome Location	chr11:9849511-9954549
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1184)
CpG islands
(count:549)
Chromatin interactive
region (count:19)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1184 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:9952406-9952773	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:9883755-9884076	K562	blood:	n/a	n/a
3	ARID3A	chr11:9927956-9928592	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:9954531-9954676	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:9878803-9879143	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:9897927-9898136	K562	blood:	n/a	n/a
7	ARID3A	chr11:9883748-9884013	HepG2	liver:	n/a	n/a
8	ATF1	chr11:9880493-9880632	K562	blood:	n/a	n/a
9	ATF1	chr11:9952454-9952810	K562	blood:	n/a	n/a
10	ATF1	chr11:9921913-9921972	K562	blood:	n/a	n/a
11	ATF1	chr11:9897920-9898187	K562	blood:	n/a	n/a
12	ATF2	chr11:9860350-9860911	GM12878	blood:	n/a	n/a
13	ATF2	chr11:9944102-9944787	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr11:9897994-9898182	K562	blood:	n/a	n/a
15	ATF3	chr11:9927327-9928521	A549	lung:	n/a	n/a
16	ATF3	chr11:9927407-9928463	A549	lung:	n/a	n/a
17	BACH1	chr11:9944284-9944722	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr11:9860401-9860780	GM12878	blood:	n/a	n/a
19	BATF	chr11:9860392-9860752	GM12878	blood:	n/a	n/a
20	BCL11A	chr11:9860414-9860736	GM12878	blood:	n/a	chr11:9860433-9860442
21	BCL11A	chr11:9927609-9927908	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL11A	chr11:9860463-9860683	GM12878	blood:	n/a	n/a
23	BCL3	chr11:9927314-9928646	A549	lung:	n/a	n/a
24	BCL3	chr11:9927385-9928510	A549	lung:	n/a	n/a
25	BCLAF1	chr11:9860396-9860731	GM12878	blood:	n/a	chr11:9860433-9860442
26	BCLAF1	chr11:9883562-9884028	GM12878	blood:	n/a	n/a
27	BHLHE40	chr11:9860450-9860695	GM12878	blood:	n/a	n/a
28	BHLHE40	chr11:9883794-9883970	K562	blood:	n/a	n/a
29	BHLHE40	chr11:9897892-9898278	K562	blood:	n/a	n/a
30	BHLHE40	chr11:9883734-9883955	HepG2	liver:	n/a	n/a
31	BRCA1	chr11:9927489-9928472	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr11:9921638-9922217	HCT-116	colon:	n/a	n/a
33	CBX3	chr11:9927406-9928048	HCT-116	colon:	n/a	chr11:9927755-9927766
34	CEBPB	chr11:9855832-9856146	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr11:9927557-9928292	IMR90	lung:	n/a	chr11:9928085-9928096 chr11:9928087-9928098 chr11:9928085-9928098 chr11:9928085-9928098 chr11:9928087-9928098
36	CEBPB	chr11:9877513-9877841	IMR90	lung:	n/a	n/a
37	CEBPB	chr11:9923452-9923765	HepG2	liver:	n/a	chr11:9923594-9923605
38	CEBPB	chr11:9905611-9905903	IMR90	lung:	n/a	chr11:9905735-9905746 chr11:9905736-9905747
39	CEBPB	chr11:9884408-9884801	Hela-S3	cervix:	n/a	chr11:9884661-9884674 chr11:9884413-9884426 chr11:9884661-9884672 chr11:9884532-9884545
40	CEBPB	chr11:9905580-9905871	K562	blood:	n/a	chr11:9905735-9905746 chr11:9905736-9905747
41	CEBPB	chr11:9927550-9928391	A549	lung:	n/a	chr11:9928085-9928096 chr11:9928087-9928098 chr11:9928085-9928098 chr11:9928085-9928098 chr11:9928087-9928098
42	CEBPB	chr11:9865891-9866134	HepG2	liver:	n/a	n/a
43	CEBPB	chr11:9905566-9905911	HepG2	liver:	n/a	chr11:9905735-9905746 chr11:9905736-9905747
44	CEBPB	chr11:9883849-9883960	K562	blood:	n/a	chr11:9883913-9883926
45	CEBPB	chr11:9868741-9868941	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr11:9927524-9928511	MCF-7	breast:	n/a	chr11:9928085-9928096 chr11:9928087-9928098 chr11:9928085-9928098 chr11:9928085-9928098 chr11:9928087-9928098
47	CEBPB	chr11:9954472-9954738	HepG2	liver:	n/a	chr11:9954537-9954548
48	CEBPB	chr11:9952541-9952703	K562	blood:	n/a	n/a
49	CEBPB	chr11:9923573-9923645	Hela-S3	cervix:	n/a	chr11:9923594-9923605
50	CEBPB	chr11:9927352-9928483	Hela-S3	cervix:	n/a	chr11:9928085-9928096 chr11:9928087-9928098 chr11:9928085-9928098 chr11:9928085-9928098 chr11:9928087-9928098

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:9944707-9944757	A549	lung:	n/a
2	chr11:9944707-9944757	PFSK-1	brain:	n/a
3	chr11:9880619-9880669	K562	blood:	n/a
4	chr11:9880619-9880669	MCF10A-Er-Src	breast:	n/a
5	chr11:9880619-9880669	HEK293	kidney:	embryo
6	chr11:9880619-9880669	AG10803	skin:	n/a
7	chr11:9915200-9915250	NHDF-neo	bronchial:	n/a
8	chr11:9860910-9860960	NHDF-neo	bronchial:	n/a
9	chr11:9915200-9915250	HEK293	kidney:	embryo
10	chr11:9879023-9879073	ovcar-3	ovarian:	n/a
11	chr11:9880619-9880669	HRPEpiC	eye:	n/a
12	chr11:9884897-9884947	H1-hESC	embryonic stem cell:	embryo
13	chr11:9884649-9884699	AoSMC	blood vessel:	n/a
14	chr11:9884649-9884699	HEK293	kidney:	embryo
15	chr11:9907493-9907543	IMR90	lung:	fetal
16	chr11:9907493-9907543	HIPEpiC	eye:	n/a
17	chr11:9884897-9884947	Caco-2	colon:	n/a
18	chr11:9907493-9907543	A549	lung:	n/a
19	chr11:9897069-9897119	AG09309	skin:	n/a
20	chr11:9944707-9944757	GM12892	blood:	n/a
21	chr11:9879023-9879073	AoSMC	blood vessel:	n/a
22	chr11:9860910-9860960	HEK293	kidney:	embryo
23	chr11:9884649-9884699	K562	blood:	n/a
24	chr11:9880619-9880669	ovcar-3	ovarian:	n/a
25	chr11:9907493-9907543	AG09309	skin:	n/a
26	chr11:9907493-9907543	GM06990	blood:	n/a
27	chr11:9884897-9884947	HCF	heart:	n/a
28	chr11:9907493-9907543	PANC-1	pancreas:	n/a
29	chr11:9879023-9879073	HCT-116	colon:	n/a
30	chr11:9884649-9884699	MCF10A-Er-Src	breast:	n/a
31	chr11:9880619-9880669	LNCaP	prostate:	n/a
32	chr11:9907493-9907543	NT2-D1	testis:	n/a
33	chr11:9860910-9860960	HCPEpiC	choroid plexus:	n/a
34	chr11:9884897-9884947	HNPCEpiC	eye:	n/a
35	chr11:9884649-9884699	MCF-7	breast:	n/a
36	chr11:9897069-9897119	HRPEpiC	eye:	n/a
37	chr11:9880619-9880669	NHDF-neo	bronchial:	n/a
38	chr11:9880619-9880669	HCT-116	colon:	n/a
39	chr11:9879023-9879073	HIPEpiC	eye:	n/a
40	chr11:9880619-9880669	ProgFib	skin:	n/a
41	chr11:9907493-9907543	MCF10A-Er-Src	breast:	n/a
42	chr11:9879023-9879073	ProgFib	skin:	n/a
43	chr11:9879023-9879073	HRPEpiC	eye:	n/a
44	chr11:9880619-9880669	HUVEC	blood vessel:	n/a
45	chr11:9884897-9884947	SAEC	small airway:	n/a
46	chr11:9860910-9860960	HPAEpiC	pulmonary alveolar:	n/a
47	chr11:9884649-9884699	ovcar-3	ovarian:	n/a
48	chr11:9897069-9897119	Hepatocyte	liver:	n/a
49	chr11:9879023-9879073	AG04449	skin:	fetal
50	chr11:9884649-9884699	RPTEC	kidney:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:9926719..9929001-chr11:10324531..10327507,2	MCF-7	breast:
2	chr11:9878394..9880153-chr11:10314990..10317190,2	K562	blood:
3	chr11:9883445..9884416-chr11:9994096..9994928,3	MCF-7	breast:
4	chr11:9868824..9871415-chr11:9878281..9879857,2	MCF-7	breast:
5	chr11:9901256..9903580-chr11:9906386..9907985,2	MCF-7	breast:
6	chr11:9883380..9884276-chr11:9994232..9995105,4	MCF-7	breast:
7	chr11:9928185..9930607-chr11:9931281..9933826,2	MCF-7	breast:
8	chr11:9918384..9921801-chr11:9925480..9929741,5	MCF-7	breast:
9	chr11:9849633..9851299-chr11:9859618..9861347,2	K562	blood:
10	chr11:9844266..9846481-chr11:9866662..9869256,2	MCF-7	breast:
11	chr11:9837195..9840045-chr11:9851275..9853158,2	K562	blood:
12	chr11:9779384..9779925-chr11:9883445..9884291,2	K562	blood:
13	chr11:9918384..9921801-chr11:9925480..9929741,5	MCF-7	breast:
14	chr11:9901256..9903580-chr11:9906386..9907985,2	MCF-7	breast:
15	chr11:9849633..9851299-chr11:9859618..9861347,2	K562	blood:
16	chr11:9868824..9871415-chr11:9878281..9879857,2	MCF-7	breast:
17	chr11:9780076..9783440-chr11:9887895..9890537,3	MCF-7	breast:
18	chr11:9928185..9930607-chr11:9931281..9933826,2	MCF-7	breast:
19	chr11:9926975..9929844-chr11:10324322..10328573,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SWAP70-2	chr11:9860690-9860823	ENSG00000255476.1
2	lnc-SWAP70-2	chr11:9950437-9950810	ENSG00000255476.1
3	lnc-SWAP70-2	chr11:9937153-9937230	ENSG00000255476.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SBF2	hsa-miR-335-5p	chr11:9860188-9860210

Variant related genes	Relation type
ENSG00000255476	TF binding region
SBF2	TF binding region
RNU7-28P	TF binding region
ENSG00000255476	CpG island
SBF2	CpG island
RNU7-28P	CpG island
ENSG00000255476	chromatin interactions
ENSG00000148926	chromatin interactions
ENSG00000133812	chromatin interactions
ENSG00000245522	chromatin interactions
ENSG00000246273	chromatin interactions
ENSG00000254554	chromatin interactions

Extended variants
information (count: 4266 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4266 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545086021	chr11:9849524-9849525	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs191644848	chr11:9849563-9849564	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572184321	chr11:9849590-9849591	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143066202	chr11:9849600-9849601	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144376756	chr11:9849641-9849642	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs529895108	chr11:9849723-9849724	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs543313669	chr11:9849744-9849745	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs184092358	chr11:9849798-9849799	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs148775380	chr11:9849839-9849840	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs533298926	chr11:9849840-9849841	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs531651890	chr11:9849875-9849876	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs188630151	chr11:9849987-9849988	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs527839046	chr11:9850002-9850003	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs565267428	chr11:9850011-9850012	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs527811398	chr11:9850060-9850061	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs547977266	chr11:9850069-9850070	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs181650061	chr11:9850087-9850088	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs546754389	chr11:9850096-9850097	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs567869479	chr11:9850138-9850139	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs185204696	chr11:9850156-9850157	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs550543560	chr11:9850187-9850188	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs190437632	chr11:9850260-9850261	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs182321172	chr11:9850272-9850273	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs186035488	chr11:9850291-9850292	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs558545046	chr11:9850339-9850340	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs572011232	chr11:9850413-9850414	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs534418690	chr11:9850426-9850427	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs566586139	chr11:9850474-9850475	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs112288069	chr11:9850503-9850504	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs543301356	chr11:9850555-9850556	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs563472328	chr11:9850592-9850593	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs576365514	chr11:9850624-9850625	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs74578546	chr11:9850668-9850669	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs565299399	chr11:9850684-9850685	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs189974254	chr11:9850704-9850705	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs553448848	chr11:9850781-9850782	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs561465186	chr11:9850791-9850792	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs577921799	chr11:9850821-9850822	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs535709324	chr11:9850839-9850840	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs372626195	chr11:9850864-9850865	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs150862959	chr11:9850865-9850866	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs570224322	chr11:9850867-9850868	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs181193289	chr11:9850868-9850869	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs369546967	chr11:9850874-9850875	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs372108899	chr11:9850878-9850879	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs375141782	chr11:9850932-9850933	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs149207066	chr11:9850936-9850937	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs368392902	chr11:9850938-9850939	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs139967004	chr11:9850942-9850943	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs534407041	chr11:9850958-9850959	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	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
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2319 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9812200-9862200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr11:9818600-9881400	Weak transcription	Spleen	Spleen
3	chr11:9824200-9867600	Weak transcription	Psoas Muscle	Psoas
4	chr11:9826800-9868200	Weak transcription	Aorta	Aorta
5	chr11:9829600-9853000	Weak transcription	Brain Angular Gyrus	brain
6	chr11:9829600-9853000	Weak transcription	Brain Substantia Nigra	brain
7	chr11:9829600-9865600	Weak transcription	Gastric	stomach
8	chr11:9829800-9853000	Weak transcription	Primary hematopoietic stem cells	blood
9	chr11:9830000-9860000	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr11:9830000-9860800	Weak transcription	Primary T cells from cord blood	blood
11	chr11:9830000-9864400	Weak transcription	Esophagus	oesophagus
12	chr11:9830200-9853200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr11:9830200-9863000	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr11:9830400-9852800	Weak transcription	Lung	lung
15	chr11:9830400-9860400	Weak transcription	Primary B cells from cord blood	blood
16	chr11:9830400-9860400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr11:9830400-9860400	Weak transcription	Brain Cingulate Gyrus	brain
18	chr11:9830400-9860400	Weak transcription	Duodenum Mucosa	Duodenum
19	chr11:9830400-9860800	Weak transcription	Rectal Smooth Muscle	rectum
20	chr11:9830400-9880400	Weak transcription	Thymus	Thymus
21	chr11:9830600-9860400	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr11:9830800-9860600	Weak transcription	Colon Smooth Muscle	Colon
23	chr11:9830800-9865600	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr11:9830800-9866800	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr11:9830800-9880600	Weak transcription	Fetal Brain Male	brain
26	chr11:9833200-9852800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr11:9833400-9868400	Weak transcription	Fetal Kidney	kidney
28	chr11:9833600-9852800	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr11:9833600-9878800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr11:9834200-9852800	Weak transcription	Dnd41	blood
31	chr11:9834200-9876600	Weak transcription	Brain Germinal Matrix	brain
32	chr11:9834400-9851400	Weak transcription	Fetal Muscle Trunk	muscle
33	chr11:9834400-9852800	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr11:9834400-9860600	Weak transcription	Brain Anterior Caudate	brain
35	chr11:9834600-9852600	Weak transcription	Stomach Smooth Muscle	stomach
36	chr11:9834600-9852800	Weak transcription	Liver	Liver
37	chr11:9834600-9852800	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr11:9834600-9853200	Weak transcription	Colonic Mucosa	Colon
39	chr11:9834600-9856000	Weak transcription	Fetal Brain Female	brain
40	chr11:9834600-9867400	Weak transcription	Brain Hippocampus Middle	brain
41	chr11:9834600-9877200	Weak transcription	Right Ventricle	heart
42	chr11:9834800-9852800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:9834800-9853000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr11:9835200-9852600	Weak transcription	Left Ventricle	heart
45	chr11:9835400-9852600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr11:9835400-9860400	Weak transcription	Fetal Stomach	stomach
47	chr11:9837600-9860400	Weak transcription	HSMMtube	muscle
48	chr11:9837600-9863200	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr11:9837600-9885800	Weak transcription	Hela-S3	cervix
50	chr11:9838000-9849600	Weak transcription	HSMM	muscle

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