Variant report

Variant	esv1810183
Chromosome Location	chr11:9323886-9334961
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:36)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:36 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:9324133-9324152	K562	blood:	n/a	n/a
2	CEBPB	chr11:9329283-9329487	K562	blood:	n/a	n/a
3	CEBPB	chr11:9334291-9334565	K562	blood:	n/a	n/a
4	CEBPB	chr11:9329309-9329455	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr11:9325320-9325470	HFF-Myc	foreskin:	n/a	n/a
6	E2F4	chr11:9333724-9333737	MCF10A-Er-Src	breast:	n/a	n/a
7	HCFC1	chr11:9334920-9337042	Hela-S3	cervix:	n/a	n/a
8	MAFF	chr11:9325813-9326013	HepG2	liver:	n/a	chr11:9325924-9325942
9	MAFF	chr11:9324118-9324321	K562	blood:	n/a	n/a
10	MAFF	chr11:9325781-9325985	K562	blood:	n/a	chr11:9325924-9325942
11	MAFK	chr11:9324078-9324379	IMR90	lung:	n/a	n/a
12	MAFK	chr11:9325791-9326076	IMR90	lung:	n/a	chr11:9325925-9325940 chr11:9325920-9325940 chr11:9325922-9325938
13	MAFK	chr11:9325776-9325990	HepG2	liver:	n/a	chr11:9325925-9325940 chr11:9325920-9325940 chr11:9325922-9325938
14	MAFK	chr11:9325809-9326012	K562	blood:	n/a	chr11:9325925-9325940 chr11:9325920-9325940 chr11:9325922-9325938
15	MAFK	chr11:9325777-9326080	HepG2	liver:	n/a	chr11:9325925-9325940 chr11:9325920-9325940 chr11:9325922-9325938
16	MAFK	chr11:9324135-9324297	K562	blood:	n/a	n/a
17	MXI1	chr11:9328713-9328767	GM12878	blood:	n/a	n/a
18	MYC	chr11:9334879-9334902	MCF10A-Er-Src	breast:	n/a	n/a
19	NFYB	chr11:9330145-9330441	Hela-S3	cervix:	n/a	chr11:9330279-9330291 chr11:9330280-9330295 chr11:9330282-9330292 chr11:9330280-9330295 chr11:9330277-9330292
20	NFYB	chr11:9330175-9330430	GM12878	blood:	n/a	chr11:9330279-9330291 chr11:9330280-9330295 chr11:9330282-9330292 chr11:9330280-9330295 chr11:9330277-9330292
21	POLR2A	chr11:9327667-9327683	HepG2	liver:	n/a	n/a
22	POLR2A	chr11:9333964-9333972	K562	blood:	n/a	n/a
23	POLR2A	chr11:9324414-9324490	K562	blood:	n/a	n/a
24	POLR2A	chr11:9326088-9326179	K562	blood:	n/a	n/a
25	POLR2A	chr11:9333388-9334108	K562	blood:	n/a	n/a
26	POLR2A	chr11:9333488-9333987	GM12878	blood:	n/a	n/a
27	POLR2A	chr11:9332635-9333711	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr11:9333674-9334103	A549	lung:	n/a	n/a
29	POLR2A	chr11:9334046-9334062	K562	blood:	n/a	n/a
30	POLR2A	chr11:9334013-9334037	K562	blood:	n/a	n/a
31	POLR2A	chr11:9332497-9332825	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr11:9324138-9324188	K562	blood:	n/a	n/a
33	POLR2A	chr11:9332727-9332735	K562	blood:	n/a	n/a
34	YY1	chr11:9332233-9332399	K562	blood:	n/a	chr11:9332320-9332328 chr11:9332316-9332332 chr11:9332321-9332331
35	ZNF384	chr11:9332074-9332420	GM12878	blood:	n/a	n/a
36	ZNF384	chr11:9332005-9332450	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:9333358-9333408	SKMC	muscle:	n/a
2	chr11:9333358-9333408	ECC-1	luminal epithelium:	n/a
3	chr11:9333358-9333408	NHDF-neo	bronchial:	n/a
4	chr11:9333358-9333408	GM12878	blood:	n/a
5	chr11:9333358-9333408	PANC-1	pancreas:	n/a
6	chr11:9333358-9333408	AG10803	skin:	n/a
7	chr11:9333358-9333408	Caco-2	colon:	n/a
8	chr11:9333358-9333408	GM06990	blood:	n/a
9	chr11:9333358-9333408	Hela-S3	cervix:	n/a
10	chr11:9333358-9333408	HNPCEpiC	eye:	n/a
11	chr11:9333358-9333408	HPAEpiC	pulmonary alveolar:	n/a
12	chr11:9333358-9333408	HL-60	blood:	n/a
13	chr11:9333358-9333408	HCPEpiC	choroid plexus:	n/a
14	chr11:9333358-9333408	A549	lung:	n/a
15	chr11:9333358-9333408	RPTEC	kidney:	n/a
16	chr11:9333358-9333408	CMK	blood:	n/a
17	chr11:9333358-9333408	Hepatocyte	liver:	n/a
18	chr11:9333358-9333408	NH-A	brain:	n/a
19	chr11:9333358-9333408	AG09319	gingival:	n/a
20	chr11:9333358-9333408	SAEC	small airway:	n/a
21	chr11:9333358-9333408	LNCaP	prostate:	n/a
22	chr11:9333358-9333408	H1-hESC	embryonic stem cell:	embryo
23	chr11:9333358-9333408	AoSMC	blood vessel:	n/a
24	chr11:9333358-9333408	IMR90	lung:	fetal
25	chr11:9333358-9333408	U87	brain:	n/a
26	chr11:9333358-9333408	ProgFib	skin:	n/a
27	chr11:9333358-9333408	K562	blood:	n/a
28	chr11:9333358-9333408	T-47D	breast:	n/a
29	chr11:9333358-9333408	HRPEpiC	eye:	n/a
30	chr11:9333358-9333408	HepG2	liver:	n/a
31	chr11:9333358-9333408	HRCEpiC	kidney:	n/a
32	chr11:9333358-9333408	PrEC	prostate:	n/a
33	chr11:9333358-9333408	HUVEC	blood vessel:	n/a
34	chr11:9333358-9333408	PFSK-1	brain:	n/a
35	chr11:9333358-9333408	HEK293	kidney:	embryo
36	chr11:9333358-9333408	BJ	skin:	n/a
37	chr11:9333358-9333408	HCM	heart:	n/a
38	chr11:9333358-9333408	HMEC	breast:	n/a
39	chr11:9333358-9333408	GM12892	blood:	n/a
40	chr11:9333358-9333408	GM19239	blood:	n/a
41	chr11:9333358-9333408	HCF	heart:	n/a
42	chr11:9333358-9333408	NB4	blood:	n/a
43	chr11:9333358-9333408	GM12891	blood:	n/a
44	chr11:9333358-9333408	Jurkat	blood:	n/a
45	chr11:9333358-9333408	SK-N-MC	brain:	n/a
46	chr11:9333358-9333408	ovcar-3	ovarian:	n/a
47	chr11:9333358-9333408	HCT-116	colon:	n/a
48	chr11:9333358-9333408	SK-N-SH_RA	brain:	n/a
49	chr11:9333358-9333408	AG09309	skin:	n/a
50	chr11:9333358-9333408	HAEpiC	amniotic membrane:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:9323308..9325382-chr11:9329913..9332100,2	K562	blood:
2	chr11:9326826..9328669-chr11:9330694..9332491,2	K562	blood:
3	chr11:9333302..9335667-chr11:9353221..9354766,2	K562	blood:
4	chr11:9316943..9319199-chr11:9321655..9323938,2	K562	blood:
5	chr11:9334944..9338278-chr11:9404354..9407861,9	MCF-7	breast:
6	chr11:9328102..9338305-chr11:9404480..9412498,38	K562	blood:
7	chr11:8985177..8988020-chr11:9331940..9333549,2	K562	blood:
8	chr11:9328690..9334073-chr11:9404480..9408917,7	K562	blood:
9	chr11:9329616..9332510-chr11:9482010..9484276,2	K562	blood:
10	chr11:9328481..9330937-chr11:9481410..9482943,2	MCF-7	breast:
11	chr11:9283945..9288774-chr11:9332278..9339081,12	K562	blood:
12	chr11:9326826..9328669-chr11:9330694..9332491,2	K562	blood:
13	chr11:9333668..9337804-chr11:9478729..9484496,11	K562	blood:
14	chr11:9334942..9338160-chr11:9405201..9408296,5	MCF-7	breast:
15	chr11:9334187..9337944-chr11:9481178..9484496,6	K562	blood:
16	chr11:9334169..9339249-chr11:9404487..9409469,24	K562	blood:
17	chr11:9321121..9324155-chr11:9406069..9408356,3	K562	blood:
18	chr11:9320121..9324688-chr11:9334835..9338165,5	K562	blood:
19	chr11:9324025..9326025-chr11:9386165..9388976,2	K562	blood:
20	chr11:9323308..9325382-chr11:9329913..9332100,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000254884	TF binding region
ENSG00000254884	CpG island
ENSG00000184014	chromatin interactions
ENSG00000166478	chromatin interactions
ENSG00000268403	chromatin interactions
ENSG00000205339	chromatin interactions
ENSG00000254860	chromatin interactions
ENSG00000175348	chromatin interactions
ENSG00000166471	chromatin interactions

Extended variants
information (count: 474 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551398449	chr11:9323894-9323895	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs56081129	chr11:9324017-9324018	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs534493674	chr11:9324081-9324082	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs146613463	chr11:9324115-9324116	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs547577525	chr11:9324128-9324129	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs567449340	chr11:9324132-9324133	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs148758074	chr11:9324170-9324171	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs66462604	chr11:9324225-9324226	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs369630305	chr11:9324364-9324365	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs192215780	chr11:9324393-9324394	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs4910449	chr11:9324394-9324395	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs184672323	chr11:9324527-9324528	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs376447274	chr11:9324557-9324558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs541310954	chr11:9324578-9324579	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs79139543	chr11:9324593-9324594	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs556150248	chr11:9324599-9324600	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs575996116	chr11:9324602-9324603	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs12275013	chr11:9324615-9324616	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs12287829	chr11:9324627-9324628	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs12287830	chr11:9324633-9324634	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs7945494	chr11:9324650-9324651	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs574692860	chr11:9324699-9324700	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543596503	chr11:9324736-9324737	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563763506	chr11:9324747-9324748	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370674413	chr11:9324754-9324755	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577170385	chr11:9324755-9324756	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546148980	chr11:9324776-9324777	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369360159	chr11:9324785-9324786	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565045546	chr11:9324808-9324809	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs79556419	chr11:9324819-9324820	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547693129	chr11:9324833-9324834	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561113532	chr11:9324875-9324876	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529904496	chr11:9324918-9324919	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549618717	chr11:9324938-9324939	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569706167	chr11:9324962-9324963	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs10743102	chr11:9325007-9325008	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs552184726	chr11:9325008-9325009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189386804	chr11:9325103-9325104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565315171	chr11:9325154-9325155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535034353	chr11:9325183-9325184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377254278	chr11:9325191-9325192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368861190	chr11:9325197-9325198	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs137935532	chr11:9325198-9325199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200364020	chr11:9325217-9325218	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs71062827	chr11:9325218-9325219	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147649845	chr11:9325224-9325225	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182082228	chr11:9325244-9325245	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs537606358	chr11:9325253-9325254	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10770014	chr11:9325260-9325261	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs577231115	chr11:9325307-9325308	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9287400-9332600	Weak transcription	HMEC	breast
2	chr11:9287400-9333000	Weak transcription	Gastric	stomach
3	chr11:9287800-9328400	Weak transcription	A549	lung
4	chr11:9287800-9333800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr11:9296600-9332600	Weak transcription	Right Ventricle	heart
6	chr11:9296600-9333000	Weak transcription	Psoas Muscle	Psoas
7	chr11:9296600-9334800	Weak transcription	Aorta	Aorta
8	chr11:9296800-9332800	Weak transcription	Brain Angular Gyrus	brain
9	chr11:9296800-9333200	Weak transcription	Colon Smooth Muscle	Colon
10	chr11:9296800-9333200	Weak transcription	Ovary	ovary
11	chr11:9302200-9324800	Weak transcription	Fetal Brain Male	brain
12	chr11:9302600-9325200	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr11:9302600-9332600	Weak transcription	Esophagus	oesophagus
14	chr11:9302600-9333200	Weak transcription	Spleen	Spleen
15	chr11:9302600-9333400	Weak transcription	Fetal Brain Female	brain
16	chr11:9302600-9333600	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr11:9302600-9334600	Weak transcription	Primary hematopoietic stem cells	blood
18	chr11:9302600-9334800	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr11:9302800-9334600	Weak transcription	NH-A	brain
20	chr11:9303200-9332000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr11:9303200-9333000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr11:9303400-9334000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr11:9305800-9332800	Weak transcription	NHDF-Ad	bronchial
24	chr11:9306000-9332600	Weak transcription	Brain Germinal Matrix	brain
25	chr11:9308000-9325000	Weak transcription	Brain Cingulate Gyrus	brain
26	chr11:9308200-9329200	Weak transcription	Brain Hippocampus Middle	brain
27	chr11:9308200-9332600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr11:9308200-9334800	Weak transcription	Primary B cells from cord blood	blood
29	chr11:9308400-9324000	Weak transcription	Stomach Smooth Muscle	stomach
30	chr11:9309400-9333800	Weak transcription	Adipose Nuclei	Adipose
31	chr11:9310000-9328400	Weak transcription	Fetal Heart	heart
32	chr11:9311400-9325000	Weak transcription	Colonic Mucosa	Colon
33	chr11:9311600-9324000	Weak transcription	GM12878-XiMat	blood
34	chr11:9312000-9331800	Weak transcription	HepG2	liver
35	chr11:9312600-9333200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr11:9312600-9334600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr11:9315000-9329800	Weak transcription	K562	blood
38	chr11:9316400-9332600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr11:9317000-9334800	Weak transcription	Placenta	Placenta
40	chr11:9317600-9325200	Weak transcription	Lung	lung
41	chr11:9318600-9329800	Weak transcription	HSMM	muscle
42	chr11:9318800-9332600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr11:9318800-9333200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr11:9319600-9330400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr11:9319600-9332600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr11:9319600-9332600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr11:9319600-9333800	Weak transcription	NHLF	lung
48	chr11:9319800-9332600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr11:9319800-9333800	Weak transcription	Primary B cells from peripheral blood	blood
50	chr11:9319800-9334800	Weak transcription	Fetal Intestine Large	intestine

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