Variant report

Variant	rs2230070
Chromosome Location	chr8:11705282-11705283
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:80)
CpG islands
(count:0)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:80 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr8:11700476-11706879	K562	blood:	n/a	n/a
2	POLR2A	chr8:11703953-11706886	K562	blood:	n/a	n/a
3	POLR2A	chr8:11702599-11705886	K562	blood:	n/a	n/a
4	POLR2A	chr8:11704688-11705987	H1-neurons	neurons:	n/a	n/a
5	POLR2A	chr8:11704720-11705468	MCF-7	breast:	n/a	n/a
6	POLR2A	chr8:11703978-11705564	HepG2	liver:	n/a	n/a
7	POLR2A	chr8:11704675-11705640	GM12892	blood:	n/a	n/a
8	HEY1	chr8:11701242-11707121	HepG2	liver:	n/a	n/a
9	JUND	chr8:11705071-11705465	HepG2	liver:	n/a	n/a
10	BCL3	chr8:11705132-11705635	K562	blood:	n/a	n/a
11	POLR2A	chr8:11703908-11707605	SK-N-MC	brain:	n/a	n/a
12	POLR2A	chr8:11703992-11706940	U87	brain:	n/a	n/a
13	CCNT2	chr8:11704199-11705839	K562	blood:	n/a	chr8:11704445-11704454 chr8:11704698-11704707 chr8:11704845-11704854
14	POLR2A	chr8:11704627-11706739	HepG2	liver:	n/a	n/a
15	POLR2A	chr8:11700572-11707656	HepG2	liver:	n/a	n/a
16	POLR2A	chr8:11700671-11705482	K562	blood:	n/a	n/a
17	POLR2A	chr8:11704074-11706942	GM19193	blood:	n/a	n/a
18	POLR2A	chr8:11703717-11706821	GM12878	blood:	n/a	n/a
19	POLR2A	chr8:11705193-11705453	A549	lung:	n/a	n/a
20	POLR2A	chr8:11703999-11706821	GM18505	blood:	n/a	n/a
21	POLR2A	chr8:11704425-11707068	ECC-1	luminal epithelium:	n/a	n/a
22	POLR2A	chr8:11700562-11707759	HepG2	liver:	n/a	n/a
23	RCOR1	chr8:11705147-11705300	HepG2	liver:	n/a	n/a
24	POLR2A	chr8:11705047-11705400	PANC-1	pancreas:	n/a	n/a
25	POLR2A	chr8:11704086-11706958	GM18951	blood:	n/a	n/a
26	POLR2A	chr8:11700619-11706983	K562	blood:	n/a	n/a
27	HMGN3	chr8:11704255-11705501	K562	blood:	n/a	n/a
28	POLR2A	chr8:11700648-11706836	K562	blood:	n/a	n/a
29	POLR2A	chr8:11703974-11705507	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr8:11705032-11706934	U87	brain:	n/a	n/a
31	POLR2A	chr8:11700677-11707213	HepG2	liver:	n/a	n/a
32	POLR2A	chr8:11700786-11707123	GM12891	blood:	n/a	n/a
33	POLR2A	chr8:11705051-11705597	GM12892	blood:	n/a	n/a
34	POLR2A	chr8:11676833-11707731	K562	blood:	n/a	n/a
35	POLR2A	chr8:11701607-11706997	HUVEC	blood vessel:	n/a	n/a
36	JUND	chr8:11705263-11705460	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr8:11704776-11705854	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr8:11704187-11705993	GM19099	blood:	n/a	n/a
39	POLR2A	chr8:11705030-11705416	HUVEC	blood vessel:	n/a	n/a
40	POLR2A	chr8:11700782-11707757	HepG2	liver:	n/a	n/a
41	POLR2A	chr8:11703989-11705534	GM12878	blood:	n/a	n/a
42	POLR2A	chr8:11704027-11705522	GM12878	blood:	n/a	n/a
43	ATF2	chr8:11704572-11705318	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr8:11700506-11713198	SK-N-MC	brain:	n/a	n/a
45	POLR2A	chr8:11701922-11707022	HL-60	blood:	n/a	n/a
46	POLR2A	chr8:11703921-11706470	HUVEC	blood vessel:	n/a	n/a
47	POLR2A	chr8:11704088-11705580	HepG2	liver:	n/a	n/a
48	POLR2A	chr8:11701479-11706769	NB4	blood:	n/a	n/a
49	JUND	chr8:11705108-11705319	HepG2	liver:	n/a	n/a
50	ZNF263	chr8:11704932-11705577	HEK293-T-REx	kidney:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:11625966..11628578-chr8:11704558..11706433,2	MCF-7	breast:

No data

Variant related genes	Relation type
CTSB	TF binding region
ENSG00000269899	TF binding region
ENSG00000154328	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10089520	1.00[CHD][hapmap]
rs1047643	1.00[CHD][hapmap]
rs17573	1.00[AMR][1000 genomes]
rs2409836	1.00[CHD][hapmap]
rs4841600	1.00[CHD][hapmap]
rs4841604	1.00[CHD][hapmap]
rs57376926	1.00[AMR][1000 genomes]
rs58313162	1.00[AMR][1000 genomes]
rs61141262	1.00[AMR][1000 genomes]
rs6981167	1.00[AMR][1000 genomes]
rs6996115	1.00[AMR][1000 genomes]
rs6998335	1.00[AMR][1000 genomes]
rs73534705	1.00[AMR][1000 genomes]
rs73534706	1.00[AMR][1000 genomes]
rs73545763	1.00[AMR][1000 genomes]
rs73545769	1.00[AMR][1000 genomes]
rs7818491	1.00[AMR][1000 genomes]
rs7823403	1.00[AMR][1000 genomes]
rs7824489	1.00[AMR][1000 genomes]
rs8191524	1.00[AMR][1000 genomes]
rs8191526	1.00[JPT][hapmap]
rs8191532	1.00[AMR][1000 genomes]
rs8191533	1.00[AMR][1000 genomes]
rs8191580	1.00[AMR][1000 genomes]
rs8191628	1.00[AMR][1000 genomes]
rs8191649	1.00[CHD][hapmap]
rs8191653	1.00[AMR][1000 genomes]
rs9886596	1.00[CHD][hapmap]

Variant overlapped rSNPs/rCNVs (count:34 , 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

No data

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	chr8:11675200-11707000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:11675800-11712600	Strong transcription	Dnd41	blood
5	chr8:11677600-11708200	Strong transcription	Cortex derived primary cultured neurospheres	brain
6	chr8:11677600-11710600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:11677600-11711800	Strong transcription	Fetal Brain Female	brain
8	chr8:11677800-11706600	Strong transcription	NHLF	lung
9	chr8:11678000-11707400	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr8:11678200-11706800	Strong transcription	H1 Cell Line	embryonic stem cell
11	chr8:11678400-11705600	Strong transcription	Fetal Muscle Trunk	muscle
12	chr8:11678400-11706400	Strong transcription	Sigmoid Colon	Sigmoid Colon
13	chr8:11678600-11705400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr8:11678600-11708600	Strong transcription	HUVEC	blood vessel
15	chr8:11679000-11715200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr8:11679200-11710400	Strong transcription	NHDF-Ad	bronchial
17	chr8:11679200-11710800	Strong transcription	Fetal Stomach	stomach
18	chr8:11679400-11705600	Strong transcription	Fetal Lung	lung
19	chr8:11680400-11706600	Strong transcription	HepG2	liver
20	chr8:11682200-11713000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
21	chr8:11682400-11712600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr8:11683000-11713200	Strong transcription	Primary B cells from peripheral blood	blood
23	chr8:11683200-11706600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr8:11683200-11710000	Strong transcription	NH-A	brain
25	chr8:11683400-11711600	Strong transcription	Brain Germinal Matrix	brain
26	chr8:11683600-11708600	Strong transcription	Primary hematopoietic stem cells	blood
27	chr8:11683600-11712600	Strong transcription	Primary neutrophils fromperipheralblood	blood
28	chr8:11685600-11710600	Strong transcription	HSMM	muscle
29	chr8:11689400-11706400	Strong transcription	Fetal Intestine Small	intestine
30	chr8:11690400-11710200	Strong transcription	Fetal Intestine Large	intestine
31	chr8:11691200-11705600	Strong transcription	Primary B cells from cord blood	blood
32	chr8:11691600-11710600	Strong transcription	Pancreas	Pancrea
33	chr8:11691600-11711200	Strong transcription	Spleen	Spleen
34	chr8:11691800-11710600	Strong transcription	HSMMtube	muscle
35	chr8:11691800-11711000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr8:11692000-11711000	Strong transcription	Fetal Muscle Leg	muscle
37	chr8:11692000-11711200	Strong transcription	Fetal Thymus	thymus
38	chr8:11692200-11711000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr8:11692400-11710600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr8:11693400-11710400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr8:11693800-11708600	Strong transcription	Aorta	Aorta
42	chr8:11694200-11706400	Strong transcription	Liver	Liver
43	chr8:11695000-11706200	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr8:11695000-11706400	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr8:11695400-11710600	Strong transcription	Osteobl	bone
46	chr8:11698600-11705600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr8:11698600-11716600	Strong transcription	Primary T cells from cord blood	blood
48	chr8:11698800-11705600	Genic enhancers	NHEK	skin
49	chr8:11698800-11711000	Strong transcription	Primary T helper cells fromperipheralblood	blood
50	chr8:11699000-11708800	Strong transcription	Ovary	ovary

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