Variant report

Variant	rs10896015
Chromosome Location	chr11:65323725-65323726
allele	A/G
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	NFIC	chr11:65323067-65323767	SK-N-SH	brain:	n/a	n/a
2	POLR2A	chr11:65322980-65323815	HUVEC	blood vessel:	n/a	n/a
3	POLR2A	chr11:65322840-65323770	HCT-116	colon:	n/a	n/a
4	JUND	chr11:65322903-65323829	HCT-116	colon:	n/a	chr11:65323483-65323493 chr11:65323215-65323227 chr11:65323483-65323493 chr11:65322962-65322971 chr11:65323482-65323493 chr11:65323480-65323491 chr11:65323483-65323493 chr11:65323217-65323225
5	POLR2A	chr11:65323497-65323736	Gliobla	brain:	n/a	n/a
6	EP300	chr11:65322976-65323812	ECC-1	luminal epithelium:	n/a	n/a
7	PBX3	chr11:65323285-65323777	SK-N-SH	brain:	n/a	n/a
8	RXRA	chr11:65323061-65323740	SK-N-SH	brain:	n/a	n/a
9	NFIC	chr11:65323156-65323737	SK-N-SH	brain:	n/a	n/a
10	POLR2A	chr11:65323138-65323772	U87	brain:	n/a	n/a
11	CEBPB	chr11:65323482-65324122	IMR90	lung:	n/a	n/a
12	PBX3	chr11:65323161-65323787	SK-N-SH	brain:	n/a	n/a
13	FOSL2	chr11:65323161-65323751	SK-N-SH	brain:	n/a	chr11:65323483-65323493 chr11:65323215-65323227 chr11:65323483-65323493 chr11:65323480-65323491 chr11:65323483-65323493 chr11:65323217-65323225
14	POLR2A	chr11:65323344-65324298	HepG2	liver:	n/a	n/a
15	EGR1	chr11:65323155-65323777	MCF-7	breast:	n/a	chr11:65323291-65323301
16	TCF12	chr11:65322958-65323832	SK-N-SH	brain:	n/a	chr11:65323277-65323287 chr11:65323285-65323295
17	FOSL2	chr11:65322952-65323775	MCF-7	breast:	n/a	chr11:65323483-65323493 chr11:65323215-65323227 chr11:65323483-65323493 chr11:65322962-65322971 chr11:65323480-65323491 chr11:65323483-65323493 chr11:65323217-65323225
18	TCF12	chr11:65323147-65323833	ECC-1	luminal epithelium:	n/a	chr11:65323277-65323287 chr11:65323285-65323295
19	FOSL2	chr11:65322960-65323761	MCF-7	breast:	n/a	chr11:65323483-65323493 chr11:65323215-65323227 chr11:65323483-65323493 chr11:65322962-65322971 chr11:65323480-65323491 chr11:65323483-65323493 chr11:65323217-65323225
20	POLR2A	chr11:65323145-65323773	HUVEC	blood vessel:	n/a	n/a
21	MAX	chr11:65323045-65323728	A549	lung:	n/a	chr11:65323217-65323226 chr11:65323443-65323453 chr11:65323292-65323302
22	EP300	chr11:65323134-65323748	SK-N-SH_RA	brain:	n/a	n/a
23	SP1	chr11:65322954-65323752	A549	lung:	n/a	chr11:65323444-65323453 chr11:65323291-65323303 chr11:65323292-65323301 chr11:65323288-65323302 chr11:65323291-65323303 chr11:65323443-65323452
24	NFIC	chr11:65323188-65323750	ECC-1	luminal epithelium:	n/a	n/a
25	EP300	chr11:65322939-65323750	A549	lung:	n/a	n/a
26	HDAC2	chr11:65323103-65323775	MCF-7	breast:	n/a	chr11:65323463-65323477
27	POLR2A	chr11:65323138-65323785	U87	brain:	n/a	n/a
28	GATA3	chr11:65323140-65323796	SK-N-SH	brain:	n/a	chr11:65323485-65323494
29	SIN3AK20	chr11:65322910-65323919	MCF-7	breast:	n/a	n/a
30	SP1	chr11:65323068-65323759	A549	lung:	n/a	chr11:65323444-65323453 chr11:65323291-65323303 chr11:65323292-65323301 chr11:65323288-65323302 chr11:65323291-65323303 chr11:65323443-65323452
31	TCF12	chr11:65323132-65323814	SK-N-SH	brain:	n/a	chr11:65323277-65323287 chr11:65323285-65323295
32	JUND	chr11:65323127-65323806	SK-N-SH	brain:	n/a	chr11:65323483-65323493 chr11:65323215-65323227 chr11:65323483-65323493 chr11:65323482-65323493 chr11:65323480-65323491 chr11:65323483-65323493 chr11:65323217-65323225
33	HDAC2	chr11:65322902-65323749	MCF-7	breast:	n/a	chr11:65323463-65323477
34	GATA3	chr11:65322976-65323807	MCF-7	breast:	n/a	chr11:65323485-65323494
35	SP1	chr11:65322871-65323836	HCT-116	colon:	n/a	chr11:65323444-65323453 chr11:65323291-65323303 chr11:65323292-65323301 chr11:65323288-65323302 chr11:65323291-65323303 chr11:65323443-65323452
36	NR2F2	chr11:65322908-65323759	MCF-7	breast:	n/a	n/a
37	FOSL2	chr11:65322952-65323772	A549	lung:	n/a	chr11:65323483-65323493 chr11:65323215-65323227 chr11:65323483-65323493 chr11:65322962-65322971 chr11:65323480-65323491 chr11:65323483-65323493 chr11:65323217-65323225
38	MAX	chr11:65323212-65323825	SK-N-SH	brain:	n/a	chr11:65323217-65323226 chr11:65323443-65323453 chr11:65323292-65323302
39	ZBTB33	chr11:65323215-65323766	HCT-116	colon:	n/a	n/a
40	EGR1	chr11:65322985-65323766	HCT-116	colon:	n/a	chr11:65323291-65323301
41	MYBL2	chr11:65323230-65323726	HepG2	liver:	n/a	n/a
42	GATA3	chr11:65322982-65323829	A549	lung:	n/a	chr11:65323485-65323494
43	RCOR1	chr11:65322901-65324417	IMR90	lung:	n/a	n/a
44	GATA3	chr11:65323138-65323747	SK-N-SH	brain:	n/a	chr11:65323485-65323494
45	JUND	chr11:65322981-65323812	SK-N-SH	brain:	n/a	chr11:65323483-65323493 chr11:65323215-65323227 chr11:65323483-65323493 chr11:65323482-65323493 chr11:65323480-65323491 chr11:65323483-65323493 chr11:65323217-65323225
46	POLR2A	chr11:65323162-65323754	SK-N-SH	brain:	n/a	n/a
47	FOSL1	chr11:65322692-65323755	HCT-116	colon:	n/a	chr11:65323483-65323493 chr11:65323215-65323227 chr11:65323483-65323493 chr11:65322962-65322971 chr11:65323480-65323491 chr11:65323483-65323493 chr11:65323217-65323225
48	MXI1	chr11:65322951-65323772	IMR90	lung:	n/a	n/a
49	MAZ	chr11:65322367-65323808	IMR90	lung:	n/a	chr11:65323217-65323226 chr11:65323443-65323453 chr11:65323292-65323302
50	EP300	chr11:65323040-65323786	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65322830..65325559-chr11:65385179..65389892,4	K562	blood:
2	chr11:65186486..65188182-chr11:65323386..65325229,2	MCF-7	breast:
3	chr11:65188903..65194388-chr11:65323256..65328284,10	MCF-7	breast:
4	chr11:65322009..65324491-chr11:65418105..65419642,2	MCF-7	breast:
5	chr11:65152331..65154319-chr11:65322563..65324840,2	K562	blood:
6	chr11:65265516..65268533-chr11:65323156..65327547,5	MCF-7	breast:
7	chr11:65322433..65324295-chr11:65381910..65384762,2	MCF-7	breast:
8	chr11:65322271..65324751-chr6:27776572..27778307,2	MCF-7	breast:
9	chr11:65189010..65195293-chr11:65321323..65327708,15	K562	blood:
10	chr11:65269130..65271131-chr11:65323511..65325144,2	MCF-7	breast:
11	chr11:65264952..65268870-chr11:65322730..65327860,7	K562	blood:
12	chr11:65264479..65268560-chr11:65318003..65330456,22	MCF-7	breast:
13	chr11:65123264..65125729-chr11:65322609..65324877,2	K562	blood:
14	chr11:65184371..65196984-chr11:65316952..65328208,29	K562	blood:

Variant related genes	Relation type
LTBP3	TF binding region
ENSG00000251562	Chromatin interaction
ENSG00000197136	Chromatin interaction
ENSG00000245532	Chromatin interaction
ENSG00000126391	Chromatin interaction
ENSG00000270117	Chromatin interaction
ENSG00000203813	Chromatin interaction
ENSG00000173327	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10896009	0.82[MEX][hapmap]
rs10896012	0.83[JPT][hapmap];0.82[MEX][hapmap]
rs10896016	0.80[JPT][hapmap]
rs11227221	0.80[JPT][hapmap]
rs1143756	0.83[ASN][1000 genomes]
rs1151496	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1151517	0.80[JPT][hapmap]
rs1152619	0.88[TSI][hapmap]
rs1152620	0.84[CEU][hapmap];0.94[TSI][hapmap]
rs11601767	0.80[JPT][hapmap];0.81[TSI][hapmap]
rs1194076	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1194077	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1194104	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12270054	1.00[ASW][hapmap];1.00[CEU][hapmap];0.86[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.94[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12360896	0.82[MEX][hapmap]
rs1346	0.89[CEU][hapmap];0.89[JPT][hapmap]
rs17146964	0.82[MEX][hapmap]
rs1783541	0.83[JPT][hapmap];0.88[MEX][hapmap];0.81[MKK][hapmap]
rs1787663	0.90[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];1.00[TSI][hapmap];0.82[ASN][1000 genomes]
rs2510078	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3200401	0.83[JPT][hapmap];0.82[MEX][hapmap]
rs3782091	0.80[JPT][hapmap]
rs4244811	0.80[JPT][hapmap]
rs600231	0.84[TSI][hapmap]
rs67924081	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs947791	0.83[JPT][hapmap];0.82[MEX][hapmap];0.81[MKK][hapmap]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897715	chr11:65083491-65427346	Enhancers Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	984 gene(s)	inside rSNPs	diseases
2	nsv897716	chr11:65083491-65481166	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	999 gene(s)	inside rSNPs	diseases
3	esv1829999	chr11:65136686-65343124	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	963 gene(s)	inside rSNPs	diseases
4	nsv897718	chr11:65140209-65577516	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1003 gene(s)	inside rSNPs	diseases
5	nsv541068	chr11:65142779-65331136	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	953 gene(s)	inside rSNPs	diseases
6	nsv541069	chr11:65142779-65368787	Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	965 gene(s)	inside rSNPs	diseases
7	nsv541070	chr11:65142779-65397058	Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	972 gene(s)	inside rSNPs	diseases
8	nsv541071	chr11:65142779-65429352	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	984 gene(s)	inside rSNPs	diseases
9	nsv897719	chr11:65157094-65335705	Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	949 gene(s)	inside rSNPs	diseases
10	nsv541073	chr11:65171202-65331136	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	949 gene(s)	inside rSNPs	diseases
11	nsv541074	chr11:65171202-65368787	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	961 gene(s)	inside rSNPs	diseases
12	nsv541075	chr11:65210592-65331136	Genic enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	620 gene(s)	inside rSNPs	diseases
13	nsv541076	chr11:65210592-65397058	Flanking Active TSS Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	645 gene(s)	inside rSNPs	diseases
14	nsv897720	chr11:65213434-65445950	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	665 gene(s)	inside rSNPs	diseases
15	nsv897721	chr11:65278461-65422853	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
16	nsv897722	chr11:65278461-65436888	Genic enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
17	nsv897723	chr11:65294830-65481166	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
18	nsv897730	chr11:65302893-65376484	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs10896015	SLC22A10	cis	parietal	SCAN
rs10896015	CDK2AP2	cis	cerebellum	SCAN
rs10896015	LTBP3	cis	cerebellum	SCAN
rs10896015	NEAT1	cis	Nerve Tibial	GTEx
rs10896015	TTC9C	cis	parietal	SCAN
rs10896015	TPCN2	cis	parietal	SCAN
rs10896015	SCGB2A1	cis	cerebellum	SCAN

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65310800-65324000	Weak transcription	Fetal Kidney	kidney
2	chr11:65318600-65325800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr11:65318800-65324600	Enhancers	Primary hematopoietic stem cells	blood
4	chr11:65319000-65324200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr11:65319000-65324600	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr11:65319000-65324600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr11:65320000-65325000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr11:65320400-65324200	Weak transcription	Aorta	Aorta
9	chr11:65320400-65324600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr11:65320400-65324600	Enhancers	Fetal Intestine Large	intestine
11	chr11:65320800-65324800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr11:65321200-65324600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr11:65321200-65324800	Enhancers	Placenta Amnion	Placenta Amnion
14	chr11:65321200-65325400	Enhancers	Fetal Brain Male	brain
15	chr11:65321200-65326200	Enhancers	Spleen	Spleen
16	chr11:65321400-65324600	Enhancers	Placenta	Placenta
17	chr11:65321400-65324800	Enhancers	Esophagus	oesophagus
18	chr11:65321600-65324000	Enhancers	HMEC	breast
19	chr11:65321600-65324200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr11:65321600-65324200	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr11:65321600-65324200	Enhancers	Fetal Thymus	thymus
22	chr11:65321600-65324200	Enhancers	Lung	lung
23	chr11:65321600-65324200	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr11:65321600-65324400	Genic enhancers	Fetal Stomach	stomach
25	chr11:65321600-65324800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr11:65321800-65323800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
27	chr11:65321800-65323800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
28	chr11:65321800-65324000	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr11:65321800-65324200	Enhancers	Colonic Mucosa	Colon
30	chr11:65321800-65324600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr11:65321800-65324600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr11:65321800-65324800	Enhancers	K562	blood
33	chr11:65321800-65325000	Enhancers	Stomach Mucosa	stomach
34	chr11:65322000-65324000	Enhancers	Colon Smooth Muscle	Colon
35	chr11:65322000-65324200	Enhancers	Primary T cells fromperipheralblood	blood
36	chr11:65322000-65324400	Enhancers	HUVEC	blood vessel
37	chr11:65322000-65324400	Enhancers	NHDF-Ad	bronchial
38	chr11:65322000-65324600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr11:65322200-65324000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr11:65322200-65324000	Enhancers	Fetal Lung	lung
41	chr11:65322200-65324200	Enhancers	Adipose Nuclei	Adipose
42	chr11:65322200-65324400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr11:65322200-65324600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr11:65322200-65324600	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr11:65322200-65325000	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr11:65322400-65323800	Flanking Active TSS	A549	lung
47	chr11:65322400-65324000	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr11:65322400-65324000	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr11:65322400-65324000	Enhancers	Brain Angular Gyrus	brain
50	chr11:65322400-65324000	Enhancers	Duodenum Smooth Muscle	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links