Variant report

Variant	esv3354083
Chromosome Location	chr11:71802283-71802674
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:71802224-71802704	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr11:71802274-71802714	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr11:71802235-71802746	GM12878	blood:	n/a	n/a
4	BCLAF1	chr11:71802302-71802699	GM12878	blood:	n/a	n/a
5	BHLHE40	chr11:71802349-71802669	K562	blood:	n/a	n/a
6	BRCA1	chr11:71802154-71802674	H1-hESC	embryonic stem cell:	n/a	n/a
7	CBX3	chr11:71802318-71802783	K562	blood:	n/a	n/a
8	CHD2	chr11:71802384-71802656	K562	blood:	n/a	n/a
9	CHD2	chr11:71802325-71802650	GM12878	blood:	n/a	n/a
10	CHD2	chr11:71802356-71802693	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr11:71802350-71802616	GM10248	blood:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
12	CTCF	chr11:71802480-71802630	HAc	cerebellar:	n/a	n/a
13	CTCF	chr11:71802420-71802570	SK-N-SH_RA	brain:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
14	CTCF	chr11:71802420-71802570	HPF	lung:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
15	CTCF	chr11:71802400-71802550	GM12865	blood:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
16	CTCF	chr11:71801781-71802912	SK-N-SH	brain:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
17	CTCF	chr11:71802400-71802550	NHDF-neo	bronchial:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
18	CTCF	chr11:71802420-71802570	Caco-2	colon:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
19	CTCF	chr11:71802420-71802570	GM12872	blood:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
20	CTCF	chr11:71802500-71802650	GM12801	blood:	n/a	n/a
21	CTCF	chr11:71802297-71802672	H1-hESC	embryonic stem cell:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
22	CTCF	chr11:71802345-71802661	Pancreas_OC	pancreas:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
23	CTCF	chr11:71802420-71802570	HBMEC	blood vessel:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
24	CTCF	chr11:71802141-71802872	HCT-116	colon:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
25	CTCF	chr11:71802326-71802660	GM12892	blood:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
26	CTCF	chr11:71802352-71802630	GM10266	blood:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
27	CTCF	chr11:71802420-71802570	GM12864	blood:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
28	CTCF	chr11:71802140-71802290	GM12873	blood:	n/a	n/a
29	CTCF	chr11:71802334-71802637	GM12891	blood:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
30	CTCF	chr11:71802420-71802570	HMF	breast:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
31	CTCF	chr11:71802440-71802590	HRE	kidney:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
32	CTCF	chr11:71802361-71802619	H1-hESC	embryonic stem cell:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
33	CTCF	chr11:71802329-71802681	MCF-7	breast:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
34	CTCF	chr11:71802400-71802550	GM12868	blood:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
35	CTCF	chr11:71802440-71802590	GM12873	blood:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
36	CTCF	chr11:71802300-71802450	HAc	cerebellar:	n/a	n/a
37	CTCF	chr11:71802440-71802590	GM12868	blood:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
38	CTCF	chr11:71802363-71802644	GM13977	blood:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
39	CTCF	chr11:71802073-71802836	MCF-7	breast:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
40	CTCF	chr11:71802420-71802570	GM12865	blood:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
41	CTCF	chr11:71802359-71802644	Hela-S3	cervix:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
42	CTCF	chr11:71802400-71802550	K562	blood:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
43	CTCF	chr11:71801735-71802913	A549	lung:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
44	CTCF	chr11:71802440-71802590	HRPEpiC	eye:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
45	CTCF	chr11:71802420-71802570	GM12874	blood:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
46	CTCF	chr11:71802347-71802645	LNCaP	prostate:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
47	CTCF	chr11:71802440-71802590	K562	blood:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
48	CTCF	chr11:71802440-71802590	Hela-S3	cervix:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
49	CTCF	chr11:71802460-71802610	MCF-7	breast:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484
50	CTCF	chr11:71802319-71802644	GM19240	blood:	n/a	chr11:71802469-71802487 chr11:71802464-71802485 chr11:71802471-71802484

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71802403-71802453	HMEC	breast:	n/a
2	chr11:71802403-71802453	HIPEpiC	eye:	n/a
3	chr11:71802403-71802453	K562	blood:	n/a
4	chr11:71802403-71802453	HCPEpiC	choroid plexus:	n/a
5	chr11:71802403-71802453	PANC-1	pancreas:	n/a
6	chr11:71802403-71802453	HEK293	kidney:	embryo
7	chr11:71802403-71802453	MCF10A-Er-Src	breast:	n/a
8	chr11:71802403-71802453	SAEC	small airway:	n/a
9	chr11:71802403-71802453	NT2-D1	testis:	n/a
10	chr11:71802403-71802453	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:71802403-71802453	AG04450	lung:	fetal
12	chr11:71802403-71802453	U87	brain:	n/a
13	chr11:71802403-71802453	GM19239	blood:	n/a
14	chr11:71802403-71802453	Caco-2	colon:	n/a
15	chr11:71802403-71802453	ProgFib	skin:	n/a
16	chr11:71802403-71802453	AG09309	skin:	n/a
17	chr11:71802403-71802453	HepG2	liver:	n/a
18	chr11:71802403-71802453	HEEpiC	esophagus:	n/a
19	chr11:71802403-71802453	NB4	blood:	n/a
20	chr11:71802403-71802453	HCF	heart:	n/a
21	chr11:71802403-71802453	HRE	kidney:	n/a
22	chr11:71802403-71802453	MCF-7	breast:	n/a
23	chr11:71802403-71802453	AoSMC	blood vessel:	n/a
24	chr11:71802403-71802453	GM12891	blood:	n/a
25	chr11:71802403-71802453	RPTEC	kidney:	n/a
26	chr11:71802403-71802453	HAEpiC	amniotic membrane:	n/a
27	chr11:71802403-71802453	A549	lung:	n/a
28	chr11:71802403-71802453	AG10803	skin:	n/a
29	chr11:71802403-71802453	T-47D	breast:	n/a
30	chr11:71802403-71802453	NHDF-neo	bronchial:	n/a
31	chr11:71802403-71802453	HRPEpiC	eye:	n/a
32	chr11:71802403-71802453	PrEC	prostate:	n/a
33	chr11:71802403-71802453	SK-N-SH_RA	brain:	n/a
34	chr11:71802403-71802453	HL-60	blood:	n/a
35	chr11:71802403-71802453	LNCaP	prostate:	n/a
36	chr11:71802403-71802453	BE2_C	brain:	n/a
37	chr11:71802403-71802453	PFSK-1	brain:	n/a
38	chr11:71802403-71802453	SK-N-SH	brain:	n/a
39	chr11:71802403-71802453	AG09319	gingival:	n/a
40	chr11:71802403-71802453	HRCEpiC	kidney:	n/a
41	chr11:71802403-71802453	Jurkat	blood:	n/a
42	chr11:71802403-71802453	CMK	blood:	n/a
43	chr11:71802403-71802453	SK-N-MC	brain:	n/a
44	chr11:71802403-71802453	Hepatocyte	liver:	n/a
45	chr11:71802403-71802453	GM06990	blood:	n/a
46	chr11:71802403-71802453	ovcar-3	ovarian:	n/a
47	chr11:71802403-71802453	Hela-S3	cervix:	n/a
48	chr11:71802403-71802453	ECC-1	luminal epithelium:	n/a
49	chr11:71802403-71802453	IMR90	lung:	fetal
50	chr11:71802403-71802453	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:71740922..71741736-chr11:71801946..71802813,2	MCF-7	breast:
2	chr11:71802059..71803123-chr11:71892536..71893396,4	MCF-7	breast:
3	chr11:71796781..71799442-chr11:71800354..71802541,3	MCF-7	breast:
4	chr11:71737643..71738177-chr11:71802084..71802697,2	MCF-7	breast:
5	chr11:71688524..71689347-chr11:71801997..71802945,2	K562	blood:
6	chr11:71801951..71802570-chr11:71894329..71895088,2	MCF-7	breast:
7	chr11:71733947..71737964-chr11:71799047..71803336,5	MCF-7	breast:
8	chr11:71735780..71737180-chr11:71801992..71803040,11	MCF-7	breast:
9	chr11:71735901..71736888-chr11:71802036..71802559,3	K562	blood:
10	chr11:71688474..71689052-chr11:71802140..71802824,2	MCF-7	breast:
11	chr11:71750983..71755251-chr11:71800972..71803523,4	MCF-7	breast:
12	chr11:71726713..71727327-chr11:71802453..71802967,2	MCF-7	breast:
13	chr11:71802021..71802787-chr17:79075240..79076177,2	MCF-7	breast:
14	chr11:71735465..71736792-chr11:71801901..71803139,15	MCF-7	breast:
15	chr11:71743810..71760160-chr11:71777190..71805714,79	MCF-7	breast:
16	chr11:71802072..71802706-chr11:72141920..72142483,2	MCF-7	breast:
17	chr11:71802429..71803055-chr11:72141805..72142468,2	MCF-7	breast:

Variant related genes	Relation type
LRTOMT	TF binding region
LRTOMT	CpG island
ENSG00000206783	chromatin interactions
ENSG00000184154	chromatin interactions
ENSG00000137497	chromatin interactions

Extended variants
information (count: 20 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143677162	chr11:71802283-71802284	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs185142340	chr11:71802317-71802318	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs565322567	chr11:71802336-71802337	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs628025	chr11:71802351-71802352	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs189855137	chr11:71802357-71802358	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs517837	chr11:71802359-71802360	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs536722159	chr11:71802368-71802369	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs548084482	chr11:71802391-71802392	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs182135280	chr11:71802401-71802402	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs533874318	chr11:71802403-71802404	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs187190370	chr11:71802404-71802405	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs146310805	chr11:71802421-71802422	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs559248786	chr11:71802481-71802482	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs537460931	chr11:71802491-71802492	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs530241009	chr11:71802498-71802499	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs201637252	chr11:71802520-71802521	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs191156342	chr11:71802532-71802533	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs574453440	chr11:71802579-71802580	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs570076239	chr11:71802601-71802602	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs183702731	chr11:71802663-71802664	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:151 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71792400-71802600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr11:71792400-71805200	Weak transcription	HSMMtube	muscle
3	chr11:71792400-71805800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr11:71792600-71802400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr11:71792600-71804200	Weak transcription	Aorta	Aorta
6	chr11:71792600-71804800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr11:71792600-71805400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr11:71792600-71805400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr11:71792600-71805400	Weak transcription	Colonic Mucosa	Colon
10	chr11:71792600-71805600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr11:71792600-71805600	Weak transcription	Esophagus	oesophagus
12	chr11:71792600-71805600	Weak transcription	Pancreas	Pancrea
13	chr11:71792600-71808800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr11:71792600-71809000	Weak transcription	Psoas Muscle	Psoas
15	chr11:71792600-71812800	Weak transcription	Fetal Heart	heart
16	chr11:71792600-71813200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr11:71792800-71804600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr11:71792800-71808200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr11:71792800-71808200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr11:71793000-71808400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr11:71793200-71808400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr11:71793400-71802600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr11:71793400-71803000	Weak transcription	GM12878-XiMat	blood
24	chr11:71793400-71805400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr11:71793800-71802400	Weak transcription	HUVEC	blood vessel
26	chr11:71796400-71807600	Weak transcription	HMEC	breast
27	chr11:71797000-71805600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr11:71797200-71804000	Weak transcription	Brain Germinal Matrix	brain
29	chr11:71797400-71808000	Weak transcription	Fetal Kidney	kidney
30	chr11:71798000-71803800	Weak transcription	Brain Angular Gyrus	brain
31	chr11:71798000-71812200	Weak transcription	Fetal Brain Male	brain
32	chr11:71798200-71805600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr11:71798600-71802400	Strong transcription	Dnd41	blood
34	chr11:71799000-71803000	Strong transcription	Fetal Stomach	stomach
35	chr11:71799000-71803400	Genic enhancers	K562	blood
36	chr11:71799200-71802800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr11:71799600-71804400	Weak transcription	Fetal Lung	lung
38	chr11:71799800-71804400	Weak transcription	Right Ventricle	heart
39	chr11:71800000-71802600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr11:71800000-71803200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr11:71800000-71805600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr11:71800200-71802800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:71800200-71804200	Weak transcription	Gastric	stomach
44	chr11:71800200-71805400	Weak transcription	NH-A	brain
45	chr11:71800200-71805600	Weak transcription	Ovary	ovary
46	chr11:71800400-71812000	Strong transcription	Primary T cells from cord blood	blood
47	chr11:71800600-71802400	Strong transcription	NHLF	lung
48	chr11:71800800-71802400	Strong transcription	HSMM	muscle
49	chr11:71801000-71802400	Strong transcription	A549	lung
50	chr11:71801000-71802800	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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