Variant report

Variant	rs2740594
Chromosome Location	chr8:11707174-11707175
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	ZNF384	chr8:11706924-11707191	K562	blood:	n/a	n/a
2	CEBPB	chr8:11707001-11707282	HepG2	liver:	n/a	chr8:11707145-11707156
3	CEBPB	chr8:11706962-11707287	ECC-1	luminal epithelium:	n/a	chr8:11707145-11707156 chr8:11706972-11706983
4	POLR2A	chr8:11703908-11707605	SK-N-MC	brain:	n/a	n/a
5	POLR2A	chr8:11700572-11707656	HepG2	liver:	n/a	n/a
6	POLR2A	chr8:11700562-11707759	HepG2	liver:	n/a	n/a
7	CEBPB	chr8:11707013-11707297	Hela-S3	cervix:	n/a	chr8:11707145-11707156
8	TEAD4	chr8:11706836-11707400	HepG2	liver:	n/a	n/a
9	POLR2A	chr8:11706425-11708174	K562	blood:	n/a	n/a
10	POLR2A	chr8:11700677-11707213	HepG2	liver:	n/a	n/a
11	POLR2A	chr8:11676833-11707731	K562	blood:	n/a	n/a
12	POLR2A	chr8:11706594-11707247	HUVEC	blood vessel:	n/a	n/a
13	POLR2A	chr8:11700782-11707757	HepG2	liver:	n/a	n/a
14	CEBPB	chr8:11707029-11707248	H1-hESC	embryonic stem cell:	n/a	chr8:11707145-11707156
15	POLR2A	chr8:11707101-11707210	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr8:11700506-11713198	SK-N-MC	brain:	n/a	n/a
17	MYC	chr8:11707067-11707249	MCF10A-Er-Src	breast:	n/a	n/a
18	CEBPB	chr8:11707051-11707253	K562	blood:	n/a	chr8:11707145-11707156
19	CEBPB	chr8:11707016-11707302	IMR90	lung:	n/a	chr8:11707145-11707156
20	CEBPB	chr8:11706904-11707252	ECC-1	luminal epithelium:	n/a	chr8:11707145-11707156 chr8:11706972-11706983
21	POLR2A	chr8:11705885-11707240	MCF10A-Er-Src	breast:	n/a	n/a
22	CEBPB	chr8:11707035-11707297	A549	lung:	n/a	chr8:11707145-11707156
23	FOSL2	chr8:11700554-11707194	HepG2	liver:	n/a	chr8:11706546-11706554 chr8:11702804-11702815
24	STAT3	chr8:11707094-11707256	MCF10A-Er-Src	breast:	n/a	n/a
25	CEBPB	chr8:11706943-11707237	HepG2	liver:	n/a	chr8:11707145-11707156 chr8:11706972-11706983
26	POLR2A	chr8:11703939-11707300	ECC-1	luminal epithelium:	n/a	n/a
27	POLR2A	chr8:11697338-11709051	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:11707017-11707237	HepG2	liver:	n/a	chr8:11707145-11707156
29	CEBPB	chr8:11706859-11707301	HepG2	liver:	n/a	chr8:11707145-11707156 chr8:11706972-11706983
30	CEBPD	chr8:11706997-11707350	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:11706290..11708186-chr8:11724044..11726922,3	MCF-7	breast:
2	chr8:11706164..11707709-chr8:11709253..11711783,2	K562	blood:
3	chr8:11664303..11666890-chr8:11705423..11707941,2	MCF-7	breast:

Variant related genes	Relation type
CTSB	TF binding region
ENSG00000269899	TF binding region
ENSG00000164733	Chromatin interaction
ENSG00000079459	Chromatin interaction

Extended variants
information (count: 76 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1122182	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11780453	1.00[ASN][1000 genomes]
rs1293289	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1293290	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1293292	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1293294	1.00[ASN][1000 genomes]
rs1293295	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1293296	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1293298	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1293300	1.00[ASN][1000 genomes]
rs1293301	1.00[ASN][1000 genomes]
rs1293308	1.00[ASN][1000 genomes]
rs1293327	1.00[ASN][1000 genomes]
rs1293331	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1296025	1.00[ASN][1000 genomes]
rs1296026	1.00[ASN][1000 genomes]
rs1692811	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1692812	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1692814	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1692817	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1692819	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1692821	1.00[ASN][1000 genomes]
rs1736065	1.00[ASN][1000 genomes]
rs1736081	1.00[ASN][1000 genomes]
rs1736082	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1736083	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1736085	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1736086	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1736089	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1736103	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2010629	1.00[ASN][1000 genomes]
rs2645417	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2645425	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2740592	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2740595	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35304870	1.00[ASN][1000 genomes]
rs3947	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4839	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs709821	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs709822	1.00[ASN][1000 genomes]
rs7831946	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1018978	chr8:11438267-11858466	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv917963	chr8:11540723-11751798	Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1027378	chr8:11541739-11858466	Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv1028229	chr8:11575762-11805961	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv539475	chr8:11575762-11805961	Flanking Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv428514	chr8:11580381-11765706	Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
8	nsv1034014	chr8:11602337-11858466	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers 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	26 gene(s)	inside rSNPs	diseases
9	nsv1023803	chr8:11623570-11721655	Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	nsv539476	chr8:11623570-11721655	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS 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	17 gene(s)	inside rSNPs	diseases
11	nsv890361	chr8:11625808-11755513	Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
12	nsv890362	chr8:11625808-11771089	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
13	nsv1032739	chr8:11643803-11716473	Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv1034132	chr8:11657033-12198242	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
15	nsv890365	chr8:11666451-11735641	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
16	nsv890366	chr8:11666451-11900847	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
17	nsv1031158	chr8:11666558-11759064	Bivalent Enhancer Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
18	nsv539477	chr8:11666558-11759064	Enhancers Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
19	nsv1018042	chr8:11667496-11882385	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
20	nsv890367	chr8:11668153-11793529	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS 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	11 gene(s)	inside rSNPs	diseases
21	nsv890368	chr8:11671041-11718528	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
22	nsv890369	chr8:11671041-11840011	Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
23	nsv1016952	chr8:11679271-11849955	Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
24	nsv1029093	chr8:11679271-11858466	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
25	nsv539478	chr8:11679271-11858466	Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
26	nsv1017334	chr8:11688534-11732949	Enhancers Active TSS Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
27	nsv539479	chr8:11688534-11732949	Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
28	nsv1019738	chr8:11696393-11732949	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
29	nsv539480	chr8:11696393-11732949	Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
30	nsv1031972	chr8:11696393-11805961	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
31	nsv539481	chr8:11696393-11805961	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
32	esv34042	chr8:11698337-11726817	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
33	nsv610293	chr8:11698747-11929734	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
34	nsv516685	chr8:11698747-12570199	Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	74 gene(s)	inside rSNPs	diseases
35	nsv972525	chr8:11706325-11714357	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2740594	CTSB	cis	Skin Sun Exposed Lower leg	GTEx
rs2740594	CTSB	cis	Artery Tibial	GTEx
rs2740594	CTSB	cis	Esophagus Muscularis	GTEx

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11667000-11711000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr8:11669400-11708000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:11675800-11712600	Strong transcription	Dnd41	blood
4	chr8:11677600-11708200	Strong transcription	Cortex derived primary cultured neurospheres	brain
5	chr8:11677600-11710600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr8:11677600-11711800	Strong transcription	Fetal Brain Female	brain
7	chr8:11678000-11707400	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr8:11678600-11708600	Strong transcription	HUVEC	blood vessel
9	chr8:11679000-11715200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr8:11679200-11710400	Strong transcription	NHDF-Ad	bronchial
11	chr8:11679200-11710800	Strong transcription	Fetal Stomach	stomach
12	chr8:11682200-11713000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
13	chr8:11682400-11712600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr8:11683000-11713200	Strong transcription	Primary B cells from peripheral blood	blood
15	chr8:11683200-11710000	Strong transcription	NH-A	brain
16	chr8:11683400-11711600	Strong transcription	Brain Germinal Matrix	brain
17	chr8:11683600-11708600	Strong transcription	Primary hematopoietic stem cells	blood
18	chr8:11683600-11712600	Strong transcription	Primary neutrophils fromperipheralblood	blood
19	chr8:11685600-11710600	Strong transcription	HSMM	muscle
20	chr8:11690400-11710200	Strong transcription	Fetal Intestine Large	intestine
21	chr8:11691600-11710600	Strong transcription	Pancreas	Pancrea
22	chr8:11691600-11711200	Strong transcription	Spleen	Spleen
23	chr8:11691800-11710600	Strong transcription	HSMMtube	muscle
24	chr8:11691800-11711000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr8:11692000-11711000	Strong transcription	Fetal Muscle Leg	muscle
26	chr8:11692000-11711200	Strong transcription	Fetal Thymus	thymus
27	chr8:11692200-11711000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr8:11692400-11710600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr8:11693400-11710400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr8:11693800-11708600	Strong transcription	Aorta	Aorta
31	chr8:11695400-11710600	Strong transcription	Osteobl	bone
32	chr8:11698600-11716600	Strong transcription	Primary T cells from cord blood	blood
33	chr8:11698800-11711000	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr8:11699000-11708800	Strong transcription	Ovary	ovary
35	chr8:11699000-11710800	Strong transcription	Primary T helper cells PMA-I stimulated	--
36	chr8:11699200-11710600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr8:11699200-11710600	Strong transcription	Muscle Satellite Cultured Cells	--
38	chr8:11699400-11710400	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr8:11700000-11711200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr8:11700600-11721200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr8:11701200-11710400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr8:11702000-11707600	Genic enhancers	HMEC	breast
43	chr8:11702200-11707800	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr8:11702200-11710400	Weak transcription	Hela-S3	cervix
45	chr8:11702400-11710000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr8:11702400-11710400	Weak transcription	Fetal Brain Male	brain
47	chr8:11702600-11710400	Weak transcription	Fetal Heart	heart
48	chr8:11703000-11708600	Genic enhancers	Placenta	Placenta
49	chr8:11703000-11721200	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr8:11703200-11708000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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