Variant report

Variant	esv3402630
Chromosome Location	chr11:8887304-8893757
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:372)
CpG islands
(count:488)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:372 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:8889450-8889730	HepG2	liver:	n/a	n/a
2	BACH1	chr11:8891972-8893157	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr11:8891806-8892323	A549	lung:	n/a	n/a
4	BDP1	chr11:8891839-8892228	Hela-S3	cervix:	n/a	n/a
5	BHLHE40	chr11:8889773-8889875	K562	blood:	n/a	n/a
6	BHLHE40	chr11:8888768-8888793	A549	lung:	n/a	n/a
7	BRCA1	chr11:8888412-8888988	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr11:8891863-8892288	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr11:8889434-8889741	HepG2	liver:	n/a	n/a
10	CEBPB	chr11:8888306-8888951	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr11:8889413-8889820	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr11:8889391-8890346	IMR90	lung:	n/a	n/a
13	CEBPB	chr11:8889429-8889750	K562	blood:	n/a	n/a
14	CEBPB	chr11:8889405-8889760	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr11:8889407-8889773	A549	lung:	n/a	n/a
16	CEBPB	chr11:8889405-8889772	A549	lung:	n/a	n/a
17	CEBPB	chr11:8889421-8889740	MCF-7	breast:	n/a	n/a
18	CEBPB	chr11:8889459-8889731	HepG2	liver:	n/a	n/a
19	CEBPB	chr11:8889462-8889674	HepG2	liver:	n/a	n/a
20	CEBPB	chr11:8889362-8889769	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr11:8891892-8892573	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr11:8889391-8889791	HepG2	liver:	n/a	n/a
23	CEBPB	chr11:8889353-8890340	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr11:8889388-8889971	A549	lung:	n/a	n/a
25	CEBPD	chr11:8889447-8889709	HepG2	liver:	n/a	chr11:8889575-8889586
26	CHD1	chr11:8892025-8892225	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr11:8893222-8893248	GM12878	blood:	n/a	n/a
28	CHD2	chr11:8891934-8892618	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr11:8888677-8888903	Hela-S3	cervix:	n/a	n/a
30	CREB1	chr11:8891932-8892272	A549	lung:	n/a	n/a
31	CREB1	chr11:8892315-8892591	A549	lung:	n/a	n/a
32	CTCF	chr11:8892039-8892297	A549	lung:	n/a	chr11:8892141-8892159
33	CTCF	chr11:8892060-8892210	AG09319	gingival:	n/a	chr11:8892141-8892159
34	CTCF	chr11:8892080-8892230	SAEC	small airway:	n/a	chr11:8892141-8892159
35	CTCF	chr11:8892087-8892228	H1-hESC	embryonic stem cell:	n/a	chr11:8892141-8892159
36	CTCF	chr11:8892040-8892190	HRE	kidney:	n/a	chr11:8892141-8892159
37	CTCF	chr11:8892106-8892204	MCF-7	breast:	n/a	chr11:8892141-8892159
38	CTCF	chr11:8892220-8892370	AG04449	skin:	n/a	n/a
39	CTCF	chr11:8892088-8892232	GM12892	blood:	n/a	chr11:8892141-8892159
40	CTCF	chr11:8888560-8888710	AG09309	skin:	n/a	n/a
41	CTCF	chr11:8893000-8893150	HBMEC	blood vessel:	n/a	chr11:8893070-8893083
42	CTCF	chr11:8892037-8892265	A549	lung:	n/a	chr11:8892141-8892159
43	CTCF	chr11:8892066-8892218	SK-N-SH_RA	brain:	n/a	chr11:8892141-8892159
44	CTCF	chr11:8892028-8892263	NHEK	skin:	n/a	chr11:8892141-8892159
45	CTCF	chr11:8892100-8892250	GM06990	blood:	n/a	chr11:8892141-8892159
46	CTCF	chr11:8892100-8892250	WERI-Rb-1	eye:	n/a	chr11:8892141-8892159
47	CTCF	chr11:8892071-8892267	GM12878	blood:	n/a	chr11:8892141-8892159
48	CTCF	chr11:8892085-8892230	Hela-S3	cervix:	n/a	chr11:8892141-8892159
49	CTCF	chr11:8893180-8893330	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr11:8892600-8892750	SK-N-SH_RA	brain:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:8888814-8888864	IMR90	lung:	fetal
2	chr11:8892893-8892943	MCF10A-Er-Src	breast:	n/a
3	chr11:8892087-8892137	HCM	heart:	n/a
4	chr11:8892893-8892943	Hela-S3	cervix:	n/a
5	chr11:8888814-8888864	AoSMC	blood vessel:	n/a
6	chr11:8891157-8891207	Jurkat	blood:	n/a
7	chr11:8892757-8892807	GM12891	blood:	n/a
8	chr11:8888703-8888753	IMR90	lung:	fetal
9	chr11:8888703-8888753	GM06990	blood:	n/a
10	chr11:8888814-8888864	NT2-D1	testis:	n/a
11	chr11:8892893-8892943	HMEC	breast:	n/a
12	chr11:8892616-8892666	H1-hESC	embryonic stem cell:	embryo
13	chr11:8888814-8888864	ECC-1	luminal epithelium:	n/a
14	chr11:8888703-8888753	ovcar-3	ovarian:	n/a
15	chr11:8892087-8892137	AoSMC	blood vessel:	n/a
16	chr11:8888703-8888753	Caco-2	colon:	n/a
17	chr11:8888814-8888864	HRPEpiC	eye:	n/a
18	chr11:8892087-8892137	MCF-7	breast:	n/a
19	chr11:8892893-8892943	HEEpiC	esophagus:	n/a
20	chr11:8888814-8888864	SKMC	muscle:	n/a
21	chr11:8888814-8888864	MCF-7	breast:	n/a
22	chr11:8891157-8891207	HAEpiC	amniotic membrane:	n/a
23	chr11:8891157-8891207	HCF	heart:	n/a
24	chr11:8892893-8892943	CMK	blood:	n/a
25	chr11:8891157-8891207	HepG2	liver:	n/a
26	chr11:8892087-8892137	AG09309	skin:	n/a
27	chr11:8891157-8891207	HCPEpiC	choroid plexus:	n/a
28	chr11:8891157-8891207	BJ	skin:	n/a
29	chr11:8892893-8892943	IMR90	lung:	fetal
30	chr11:8892760-8892810	PANC-1	pancreas:	n/a
31	chr11:8892087-8892137	NH-A	brain:	n/a
32	chr11:8892760-8892810	ProgFib	skin:	n/a
33	chr11:8892757-8892807	HRCEpiC	kidney:	n/a
34	chr11:8891157-8891207	GM19239	blood:	n/a
35	chr11:8888703-8888753	GM12878	blood:	n/a
36	chr11:8888703-8888753	CMK	blood:	n/a
37	chr11:8892893-8892943	MCF-7	breast:	n/a
38	chr11:8892893-8892943	PFSK-1	brain:	n/a
39	chr11:8892757-8892807	HEK293	kidney:	embryo
40	chr11:8892893-8892943	SK-N-SH_RA	brain:	n/a
41	chr11:8891157-8891207	SK-N-SH	brain:	n/a
42	chr11:8892616-8892666	HCT-116	colon:	n/a
43	chr11:8892893-8892943	AG10803	skin:	n/a
44	chr11:8892087-8892137	Hela-S3	cervix:	n/a
45	chr11:8892757-8892807	BE2_C	brain:	n/a
46	chr11:8892616-8892666	BE2_C	brain:	n/a
47	chr11:8891157-8891207	BE2_C	brain:	n/a
48	chr11:8892757-8892807	AG09319	gingival:	n/a
49	chr11:8892616-8892666	AG09319	gingival:	n/a
50	chr11:8892087-8892137	GM12891	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:155057376..155058095-chr11:8892407..8893076,2	Hela-S3	cervix:
2	chr11:8854026..8855722-chr11:8888927..8890740,3	MCF-7	breast:
3	chr11:8701293..8704221-chr11:8890079..8892942,2	MCF-7	breast:
4	chr11:8706918..8709095-chr11:8891415..8893255,2	MCF-7	breast:
5	chr11:8891163..8893518-chr11:8931818..8934397,2	MCF-7	breast:
6	chr11:8885722..8888540-chr11:9189607..9191630,2	K562	blood:

No data

Variant related genes	Relation type
ST5	TF binding region
ST5	CpG island
ENSG00000166444	chromatin interactions
ENSG00000166441	chromatin interactions
ENSG00000166452	chromatin interactions
ENSG00000143590	chromatin interactions
ENSG00000212607	chromatin interactions

Extended variants
information (count: 222 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:222 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576377307	chr11:8887350-8887351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs538571171	chr11:8887378-8887379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145775388	chr11:8887416-8887417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376257992	chr11:8887463-8887464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181102739	chr11:8887523-8887524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185510609	chr11:8887530-8887531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs148674730	chr11:8887532-8887533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs574202754	chr11:8887563-8887564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542964534	chr11:8887588-8887589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562964077	chr11:8887593-8887594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532016760	chr11:8887655-8887656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552576328	chr11:8887656-8887657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550854802	chr11:8887665-8887666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188728774	chr11:8887696-8887697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113531595	chr11:8887732-8887733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528671706	chr11:8887767-8887768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548774912	chr11:8887783-8887784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs77815196	chr11:8887813-8887814	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs2568062	chr11:8887945-8887946	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs373545513	chr11:8888021-8888022	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs550960258	chr11:8888042-8888043	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs570843265	chr11:8888048-8888049	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs539847528	chr11:8888054-8888055	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs181460366	chr11:8888061-8888062	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs141249206	chr11:8888081-8888082	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs185997009	chr11:8888091-8888092	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs150752136	chr11:8888169-8888170	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs574164365	chr11:8888195-8888196	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs191838480	chr11:8888196-8888197	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs543127832	chr11:8888197-8888198	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs139577929	chr11:8888201-8888202	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs576763065	chr11:8888229-8888230	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs184124621	chr11:8888280-8888281	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs559755670	chr11:8888377-8888378	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs528785366	chr11:8888519-8888520	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs375550505	chr11:8888532-8888533	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs146037484	chr11:8888541-8888542	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs145092964	chr11:8888587-8888588	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs531163290	chr11:8888639-8888640	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs564438567	chr11:8888645-8888646	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs376308876	chr11:8888649-8888650	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs185757818	chr11:8888679-8888680	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs11042103	chr11:8888700-8888701	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs77234696	chr11:8888703-8888704	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs75904758	chr11:8888739-8888740	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs58735631	chr11:8888752-8888753	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs74054241	chr11:8888753-8888754	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs568780250	chr11:8888778-8888779	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs370522239	chr11:8888840-8888841	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs377425809	chr11:8888849-8888850	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Lung cancer	18438408	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
Dysmorphic features	22052655	CNVD
Intellectual disability	22052655	CNVD
Obesity	22052655	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:585 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8862400-8888400	Weak transcription	Right Atrium	heart
2	chr11:8863200-8890400	Weak transcription	Fetal Muscle Trunk	muscle
3	chr11:8864000-8888000	Weak transcription	Fetal Intestine Small	intestine
4	chr11:8877400-8888600	Weak transcription	Fetal Muscle Leg	muscle
5	chr11:8877400-8888600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr11:8878200-8891800	Weak transcription	Psoas Muscle	Psoas
7	chr11:8880200-8892000	Weak transcription	Gastric	stomach
8	chr11:8880400-8888000	Weak transcription	Stomach Mucosa	stomach
9	chr11:8880400-8888200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr11:8880400-8889200	Weak transcription	Lung	lung
11	chr11:8881400-8888200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr11:8884200-8887800	Enhancers	Hela-S3	cervix
13	chr11:8884200-8889600	Enhancers	NHDF-Ad	bronchial
14	chr11:8884400-8889000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr11:8884400-8891800	Weak transcription	Left Ventricle	heart
16	chr11:8885000-8888200	Enhancers	NHLF	lung
17	chr11:8885200-8887400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr11:8885200-8889000	Enhancers	HUVEC	blood vessel
19	chr11:8885600-8888000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr11:8885600-8891400	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr11:8885600-8891400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr11:8885800-8888000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr11:8885800-8888400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr11:8885800-8888400	Weak transcription	A549	lung
25	chr11:8885800-8889600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr11:8885800-8889800	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr11:8885800-8889800	Weak transcription	Rectal Smooth Muscle	rectum
28	chr11:8885800-8891400	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr11:8885800-8891400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr11:8885800-8891400	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr11:8885800-8891800	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr11:8886000-8888000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr11:8886000-8888000	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr11:8886000-8888200	Weak transcription	Small Intestine	intestine
35	chr11:8886000-8888200	Weak transcription	HSMM	muscle
36	chr11:8886000-8889400	Weak transcription	HSMMtube	muscle
37	chr11:8886000-8889600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr11:8886000-8889600	Weak transcription	Ovary	ovary
39	chr11:8886200-8888000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr11:8886200-8888000	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr11:8886200-8888000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr11:8886200-8888000	Weak transcription	Placenta	Placenta
43	chr11:8886200-8888000	Weak transcription	NH-A	brain
44	chr11:8886200-8889600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr11:8886200-8889600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr11:8886400-8888200	Weak transcription	Osteobl	bone
47	chr11:8886600-8888000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr11:8886600-8888200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr11:8886600-8888400	Weak transcription	Fetal Stomach	stomach
50	chr11:8886800-8889600	Weak transcription	HUES6 Cell Line	embryonic stem cell

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