Variant report

Variant	esv1819684
Chromosome Location	chr11:9973062-10012511
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:602)
CpG islands
(count:183)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:602 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:10012155-10012488	HepG2	liver:	n/a	n/a
2	ATF1	chr11:9978223-9978390	K562	blood:	n/a	n/a
3	ATF2	chr11:9984169-9984650	GM12878	blood:	n/a	n/a
4	ATF2	chr11:9984115-9984704	GM12878	blood:	n/a	n/a
5	ATF3	chr11:10004659-10005096	A549	lung:	n/a	n/a
6	BATF	chr11:9994519-9994792	GM12878	blood:	n/a	chr11:9994688-9994697
7	BATF	chr11:9984302-9984676	GM12878	blood:	n/a	n/a
8	BCL3	chr11:10004437-10005076	A549	lung:	n/a	n/a
9	BCL3	chr11:10004548-10005126	A549	lung:	n/a	n/a
10	BCLAF1	chr11:9984166-9984674	GM12878	blood:	n/a	n/a
11	BCLAF1	chr11:9984271-9984598	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:9984365-9984604	GM12878	blood:	n/a	n/a
13	BRCA1	chr11:9994495-9994970	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr11:10004722-10005080	K562	blood:	n/a	n/a
15	CEBPB	chr11:9978063-9978347	K562	blood:	n/a	chr11:9978174-9978185
16	CEBPB	chr11:9978058-9978263	IMR90	lung:	n/a	chr11:9978174-9978185
17	CEBPB	chr11:9990638-9990986	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:9978076-9978275	K562	blood:	n/a	chr11:9978174-9978185
19	CEBPB	chr11:9994600-9994759	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr11:9994597-9994793	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr11:10004678-10005094	A549	lung:	n/a	n/a
22	CTCF	chr11:10012340-10012490	NHDF-neo	bronchial:	n/a	n/a
23	CTCF	chr11:10004980-10005130	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr11:10004778-10004967	Gliobla	brain:	n/a	n/a
25	CTCF	chr11:9994560-9994710	GM12873	blood:	n/a	n/a
26	CTCF	chr11:9994560-9994710	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr11:9995720-9995870	HUVEC	blood vessel:	n/a	n/a
28	CTCF	chr11:9994640-9994790	HCM	heart:	n/a	n/a
29	CTCF	chr11:10004811-10004983	MCF-7	breast:	n/a	n/a
30	CTCF	chr11:10012253-10012605	A549	lung:	n/a	n/a
31	CTCF	chr11:10012420-10012570	HA-sp	spinal cord:	n/a	n/a
32	CTCF	chr11:10012340-10012490	HepG2	liver:	n/a	n/a
33	CTCF	chr11:10012253-10012565	A549	lung:	n/a	n/a
34	CTCF	chr11:10012320-10012470	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr11:9994518-9994779	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr11:9994412-9994797	A549	lung:	n/a	n/a
37	CTCF	chr11:9994500-9994650	GM12867	blood:	n/a	n/a
38	CTCF	chr11:10012400-10012550	HMF	breast:	n/a	n/a
39	CTCF	chr11:10012360-10012510	AG04449	skin:	n/a	n/a
40	CTCF	chr11:9994560-9994710	HPF	lung:	n/a	n/a
41	CTCF	chr11:9994540-9994690	GM12867	blood:	n/a	n/a
42	CTCF	chr11:9994540-9994690	GM12866	blood:	n/a	n/a
43	CTCF	chr11:10012360-10012510	AG10803	skin:	n/a	n/a
44	CTCF	chr11:9994580-9994730	HMEC	breast:	n/a	n/a
45	CTCF	chr11:9994567-9994729	A549	lung:	n/a	n/a
46	CTCF	chr11:10012306-10012620	MCF-7	breast:	n/a	n/a
47	CTCF	chr11:9994520-9994670	HL-60	blood:	n/a	n/a
48	CTCF	chr11:10012360-10012510	MCF-7	breast:	n/a	n/a
49	CTCF	chr11:10012380-10012530	HVMF	connective:	n/a	n/a
50	CTCF	chr11:9994491-9994735	A549	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:10002835-10002885	A549	lung:	n/a
2	chr11:9995602-9995652	NHDF-neo	bronchial:	n/a
3	chr11:9995602-9995652	PrEC	prostate:	n/a
4	chr11:9992187-9992237	AG09309	skin:	n/a
5	chr11:9995602-9995652	SK-N-SH	brain:	n/a
6	chr11:10002835-10002885	K562	blood:	n/a
7	chr11:9995602-9995652	HCPEpiC	choroid plexus:	n/a
8	chr11:10002835-10002885	NT2-D1	testis:	n/a
9	chr11:9992187-9992237	PFSK-1	brain:	n/a
10	chr11:9995602-9995652	AoSMC	blood vessel:	n/a
11	chr11:10002835-10002885	HAEpiC	amniotic membrane:	n/a
12	chr11:9995602-9995652	GM12878	blood:	n/a
13	chr11:9992187-9992237	HRE	kidney:	n/a
14	chr11:10002835-10002885	IMR90	lung:	fetal
15	chr11:10002835-10002885	HCM	heart:	n/a
16	chr11:9995602-9995652	HL-60	blood:	n/a
17	chr11:10002835-10002885	NB4	blood:	n/a
18	chr11:9995602-9995652	ovcar-3	ovarian:	n/a
19	chr11:9995602-9995652	HUVEC	blood vessel:	n/a
20	chr11:9995602-9995652	SAEC	small airway:	n/a
21	chr11:9995602-9995652	Hela-S3	cervix:	n/a
22	chr11:10002835-10002885	PrEC	prostate:	n/a
23	chr11:9995602-9995652	AG04449	skin:	fetal
24	chr11:10002835-10002885	Hela-S3	cervix:	n/a
25	chr11:10002835-10002885	HRPEpiC	eye:	n/a
26	chr11:9995602-9995652	Hepatocyte	liver:	n/a
27	chr11:9995602-9995652	ProgFib	skin:	n/a
28	chr11:9992187-9992237	AG04449	skin:	fetal
29	chr11:9995602-9995652	AG09319	gingival:	n/a
30	chr11:9995602-9995652	SK-N-SH_RA	brain:	n/a
31	chr11:9992187-9992237	AoSMC	blood vessel:	n/a
32	chr11:10002835-10002885	AG09319	gingival:	n/a
33	chr11:9992187-9992237	BJ	skin:	n/a
34	chr11:10002835-10002885	SK-N-MC	brain:	n/a
35	chr11:9992187-9992237	T-47D	breast:	n/a
36	chr11:9995602-9995652	AG04450	lung:	fetal
37	chr11:9992187-9992237	Caco-2	colon:	n/a
38	chr11:9995602-9995652	GM12891	blood:	n/a
39	chr11:9995602-9995652	MCF-7	breast:	n/a
40	chr11:9995602-9995652	Jurkat	blood:	n/a
41	chr11:10002835-10002885	Caco-2	colon:	n/a
42	chr11:10002835-10002885	GM12878	blood:	n/a
43	chr11:10002835-10002885	AG04449	skin:	fetal
44	chr11:9992187-9992237	HCT-116	colon:	n/a
45	chr11:9992187-9992237	NHBE	bronchial:	n/a
46	chr11:9995602-9995652	HNPCEpiC	eye:	n/a
47	chr11:10002835-10002885	HRE	kidney:	n/a
48	chr11:9992187-9992237	Jurkat	blood:	n/a
49	chr11:10002835-10002885	H1-hESC	embryonic stem cell:	embryo
50	chr11:9995602-9995652	NT2-D1	testis:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:9991428..9993143-chr11:10058135..10060614,2	K562	blood:
2	chr11:10004750..10006557-chr11:10010668..10012877,2	MCF-7	breast:
3	chr11:10002720..10004321-chr11:10011527..10014066,2	K562	blood:
4	chr11:9482450..9484248-chr11:9984519..9986171,2	K562	blood:
5	chr11:10000703..10003036-chr11:10327811..10330632,2	MCF-7	breast:
6	chr11:10002720..10004321-chr11:10011527..10014066,2	K562	blood:
7	chr11:9967314..9969682-chr11:9973855..9976394,2	MCF-7	breast:
8	chr11:10010659..10013525-chr11:10017615..10019134,2	K562	blood:
9	chr11:9883380..9884276-chr11:9994232..9995105,4	MCF-7	breast:
10	chr11:9994901..9996412-chr11:10324131..10325757,2	MCF-7	breast:
11	chr11:10011394..10012992-chr11:10327878..10330326,2	MCF-7	breast:
12	chr11:9779414..9780281-chr11:9994114..9995162,4	K562	blood:
13	chr11:9994842..9997807-chr11:10313418..10316499,3	MCF-7	breast:
14	chr11:10012021..10012653-chr11:10098365..10099087,2	MCF-7	breast:
15	chr11:9883445..9884416-chr11:9994096..9994928,3	MCF-7	breast:
16	chr11:10004750..10006557-chr11:10010668..10012877,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000254765	TF binding region
SBF2	TF binding region
ENSG00000254765	CpG island
SBF2	CpG island
ENSG00000245522	chromatin interactions
ENSG00000254554	chromatin interactions
ENSG00000133805	chromatin interactions
ENSG00000166478	chromatin interactions
ENSG00000246273	chromatin interactions
ENSG00000133812	chromatin interactions

Extended variants
information (count: 1597 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1597 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10500715	chr11:9973062-9973063	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs367601693	chr11:9973068-9973069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576148402	chr11:9973098-9973099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535896182	chr11:9973113-9973114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555588606	chr11:9973115-9973116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575759167	chr11:9973186-9973187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538076934	chr11:9973221-9973222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558465599	chr11:9973232-9973233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs61876979	chr11:9973259-9973260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs578257871	chr11:9973297-9973298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7949110	chr11:9973299-9973300	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs560236160	chr11:9973300-9973301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7935235	chr11:9973303-9973304	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs542674779	chr11:9973325-9973326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141768996	chr11:9973396-9973397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531514514	chr11:9973492-9973493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7938570	chr11:9973511-9973512	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs564829800	chr11:9973520-9973521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186920236	chr11:9973531-9973532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530276596	chr11:9973551-9973552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192742931	chr11:9973557-9973558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184628395	chr11:9973617-9973618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34533325	chr11:9973655-9973656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189845978	chr11:9973657-9973658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549427874	chr11:9973675-9973676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569277557	chr11:9973710-9973711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7342224	chr11:9973750-9973751	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs192816803	chr11:9973753-9973754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533529343	chr11:9973759-9973760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534455910	chr11:9973778-9973779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200028887	chr11:9973789-9973790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186664270	chr11:9973792-9973793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200991258	chr11:9973793-9973794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369265865	chr11:9973794-9973795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200429661	chr11:9973795-9973796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78526867	chr11:9973818-9973819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs57243169	chr11:9973822-9973823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs71034748	chr11:9973826-9973827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538977611	chr11:9973876-9973877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542288641	chr11:9973888-9973889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113239472	chr11:9973895-9973896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184514027	chr11:9973962-9973963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs61876980	chr11:9973987-9973988	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs139908643	chr11:9974044-9974045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565717263	chr11:9974064-9974065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12279495	chr11:9974104-9974105	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs547253468	chr11:9974115-9974116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561047005	chr11:9974163-9974164	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371182072	chr11:9974189-9974190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549140872	chr11:9974212-9974213	Weak transcription Enhancers	n/a	n/a	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	18451855	CNVD

Chromatin state (count:951 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9894400-9978600	Weak transcription	Left Ventricle	heart
2	chr11:9943400-9980600	Weak transcription	Primary T cells from cord blood	blood
3	chr11:9950200-9980400	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr11:9952800-9980200	Weak transcription	Aorta	Aorta
5	chr11:9952800-9980400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr11:9952800-9980600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr11:9952800-9980600	Weak transcription	Spleen	Spleen
8	chr11:9952800-9995200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr11:9953000-9978200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr11:9953000-9979600	Weak transcription	Fetal Stomach	stomach
11	chr11:9953000-9980200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr11:9953000-9980200	Weak transcription	Stomach Smooth Muscle	stomach
13	chr11:9953000-9980400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr11:9953000-9980400	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr11:9953000-9980400	Weak transcription	Esophagus	oesophagus
16	chr11:9958800-9978200	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr11:9960600-9973400	Weak transcription	Fetal Heart	heart
18	chr11:9964400-9973600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr11:9964400-9980200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr11:9964800-9980400	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr11:9965200-9975600	Weak transcription	HSMM	muscle
22	chr11:9965200-9981000	Weak transcription	HUVEC	blood vessel
23	chr11:9965400-9980200	Weak transcription	Liver	Liver
24	chr11:9965600-9973200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr11:9965600-9973400	Weak transcription	A549	lung
26	chr11:9965800-9973400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr11:9966000-9975200	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr11:9966000-9975600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr11:9966000-9980200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr11:9966000-9980200	Weak transcription	NHLF	lung
31	chr11:9966200-9980200	Weak transcription	Osteobl	bone
32	chr11:9966600-9973200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr11:9967600-9980200	Weak transcription	Fetal Intestine Large	intestine
34	chr11:9967600-9980400	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr11:9967800-9973800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr11:9967800-9977800	Weak transcription	Fetal Lung	lung
37	chr11:9967800-9980200	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr11:9967800-9980200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr11:9967800-9980200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr11:9967800-9980400	Weak transcription	Primary hematopoietic stem cells	blood
41	chr11:9968000-9973200	Weak transcription	Adipose Nuclei	Adipose
42	chr11:9968000-9973400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr11:9968000-9973400	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr11:9968000-9973400	Weak transcription	Brain Anterior Caudate	brain
45	chr11:9968000-9976400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr11:9968000-9979600	Weak transcription	Fetal Muscle Leg	muscle
47	chr11:9968000-9980200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr11:9968000-9980400	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr11:9968000-9980400	Weak transcription	Dnd41	blood
50	chr11:9968000-9984000	Weak transcription	Primary B cells from cord blood	blood

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