Variant report

Variant	rs1736089
Chromosome Location	chr8:11705870-11705871
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:60)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:60 , 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	JUND	chr8:11705573-11705939	HepG2	liver:	n/a	n/a
6	HEY1	chr8:11701242-11707121	HepG2	liver:	n/a	n/a
7	POLR2A	chr8:11703908-11707605	SK-N-MC	brain:	n/a	n/a
8	POLR2A	chr8:11703992-11706940	U87	brain:	n/a	n/a
9	POLR2A	chr8:11704627-11706739	HepG2	liver:	n/a	n/a
10	POLR2A	chr8:11705625-11706244	GM12878	blood:	n/a	n/a
11	POLR2A	chr8:11700572-11707656	HepG2	liver:	n/a	n/a
12	POLR2A	chr8:11704074-11706942	GM19193	blood:	n/a	n/a
13	POLR2A	chr8:11703717-11706821	GM12878	blood:	n/a	n/a
14	POLR2A	chr8:11703999-11706821	GM18505	blood:	n/a	n/a
15	POLR2A	chr8:11704425-11707068	ECC-1	luminal epithelium:	n/a	n/a
16	POLR2A	chr8:11700562-11707759	HepG2	liver:	n/a	n/a
17	POLR2A	chr8:11704086-11706958	GM18951	blood:	n/a	n/a
18	STAT3	chr8:11705850-11705921	MCF10A-Er-Src	breast:	n/a	n/a
19	POLR2A	chr8:11700619-11706983	K562	blood:	n/a	n/a
20	POLR2A	chr8:11700648-11706836	K562	blood:	n/a	n/a
21	POLR2A	chr8:11705032-11706934	U87	brain:	n/a	n/a
22	POLR2A	chr8:11700677-11707213	HepG2	liver:	n/a	n/a
23	POLR2A	chr8:11700786-11707123	GM12891	blood:	n/a	n/a
24	MYBL2	chr8:11705608-11706163	HepG2	liver:	n/a	n/a
25	POLR2A	chr8:11676833-11707731	K562	blood:	n/a	n/a
26	POLR2A	chr8:11701607-11706997	HUVEC	blood vessel:	n/a	n/a
27	POLR2A	chr8:11704187-11705993	GM19099	blood:	n/a	n/a
28	POLR2A	chr8:11700782-11707757	HepG2	liver:	n/a	n/a
29	POLR2A	chr8:11705499-11705972	PANC-1	pancreas:	n/a	n/a
30	POLR2A	chr8:11700506-11713198	SK-N-MC	brain:	n/a	n/a
31	POLR2A	chr8:11701922-11707022	HL-60	blood:	n/a	n/a
32	POLR2A	chr8:11705832-11706881	HepG2	liver:	n/a	n/a
33	POLR2A	chr8:11703921-11706470	HUVEC	blood vessel:	n/a	n/a
34	POLR2A	chr8:11701479-11706769	NB4	blood:	n/a	n/a
35	POLR2A	chr8:11703919-11707099	HepG2	liver:	n/a	n/a
36	POLR2A	chr8:11700668-11707004	K562	blood:	n/a	n/a
37	POLR2A	chr8:11703509-11706647	PFSK-1	brain:	n/a	n/a
38	FOSL2	chr8:11700554-11707194	HepG2	liver:	n/a	chr8:11706546-11706554 chr8:11702804-11702815
39	POLR2A	chr8:11704158-11706203	A549	lung:	n/a	n/a
40	MYBL2	chr8:11705577-11705961	HepG2	liver:	n/a	n/a
41	POLR2A	chr8:11704056-11706714	HCT-116	colon:	n/a	n/a
42	NFATC1	chr8:11704653-11706140	GM12878	blood:	n/a	n/a
43	POLR2A	chr8:11701009-11707073	HL-60	blood:	n/a	n/a
44	POLR2A	chr8:11705590-11706915	MCF-7	breast:	n/a	n/a
45	CHD2	chr8:11704595-11706832	HepG2	liver:	n/a	n/a
46	POLR2A	chr8:11703750-11707099	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr8:11704029-11707068	GM12878	blood:	n/a	n/a
48	POLR2A	chr8:11705588-11706001	HepG2	liver:	n/a	n/a
49	POLR2A	chr8:11704120-11706804	GM15510	blood:	n/a	n/a
50	POLR2A	chr8:11703603-11706866	GM12878	blood:	n/a	n/a

No data

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:11662566..11665636-chr8:11705504..11707081,3	K562	blood:
2	chr8:11625966..11628578-chr8:11704558..11706433,2	MCF-7	breast:
3	chr8:11664303..11666890-chr8:11705423..11707941,2	MCF-7	breast:

No data

Variant related genes	Relation type
CTSB	TF binding region
ENSG00000269899	TF binding region
ENSG00000154328	Chromatin interaction
ENSG00000079459	Chromatin interaction

Extended variants
information (count: 81 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1122182	1.00[ASN][1000 genomes]
rs11780453	1.00[ASN][1000 genomes]
rs1293289	1.00[ASN][1000 genomes]
rs1293290	1.00[ASN][1000 genomes]
rs1293292	1.00[ASN][1000 genomes]
rs1293294	1.00[ASN][1000 genomes]
rs1293295	1.00[ASN][1000 genomes]
rs1293296	1.00[ASN][1000 genomes]
rs1293298	0.88[AMR][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]
rs1293316	0.83[EUR][1000 genomes]
rs1293322	0.84[EUR][1000 genomes]
rs1293325	0.85[EUR][1000 genomes]
rs1293326	0.81[EUR][1000 genomes]
rs1293327	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1293328	0.82[EUR][1000 genomes]
rs1293331	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1296025	1.00[ASN][1000 genomes]
rs1296026	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1296028	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1692811	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1692812	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1692814	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1692817	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1692819	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1692821	1.00[ASN][1000 genomes]
rs1736065	1.00[ASN][1000 genomes]
rs1736081	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1736082	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1736083	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1736085	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1736086	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1736103	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2010629	1.00[ASN][1000 genomes]
rs2645417	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2645425	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2740592	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2740594	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2740595	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35304870	1.00[ASN][1000 genomes]
rs3947	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4839	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs709821	0.85[AMR][1000 genomes];0.92[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: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

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs1736089	CTSB	cis	Esophagus Muscularis	GTEx
rs1736089	CTSB	cis	Artery Tibial	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	chr8:11675200-11707000	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	chr8:11678400-11706400	Strong transcription	Sigmoid Colon	Sigmoid Colon
12	chr8:11678600-11708600	Strong transcription	HUVEC	blood vessel
13	chr8:11679000-11715200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr8:11679200-11710400	Strong transcription	NHDF-Ad	bronchial
15	chr8:11679200-11710800	Strong transcription	Fetal Stomach	stomach
16	chr8:11680400-11706600	Strong transcription	HepG2	liver
17	chr8:11682200-11713000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr8:11682400-11712600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr8:11683000-11713200	Strong transcription	Primary B cells from peripheral blood	blood
20	chr8:11683200-11706600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr8:11683200-11710000	Strong transcription	NH-A	brain
22	chr8:11683400-11711600	Strong transcription	Brain Germinal Matrix	brain
23	chr8:11683600-11708600	Strong transcription	Primary hematopoietic stem cells	blood
24	chr8:11683600-11712600	Strong transcription	Primary neutrophils fromperipheralblood	blood
25	chr8:11685600-11710600	Strong transcription	HSMM	muscle
26	chr8:11689400-11706400	Strong transcription	Fetal Intestine Small	intestine
27	chr8:11690400-11710200	Strong transcription	Fetal Intestine Large	intestine
28	chr8:11691600-11710600	Strong transcription	Pancreas	Pancrea
29	chr8:11691600-11711200	Strong transcription	Spleen	Spleen
30	chr8:11691800-11710600	Strong transcription	HSMMtube	muscle
31	chr8:11691800-11711000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr8:11692000-11711000	Strong transcription	Fetal Muscle Leg	muscle
33	chr8:11692000-11711200	Strong transcription	Fetal Thymus	thymus
34	chr8:11692200-11711000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr8:11692400-11710600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr8:11693400-11710400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr8:11693800-11708600	Strong transcription	Aorta	Aorta
38	chr8:11694200-11706400	Strong transcription	Liver	Liver
39	chr8:11695000-11706200	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr8:11695000-11706400	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr8:11695400-11710600	Strong transcription	Osteobl	bone
42	chr8:11698600-11716600	Strong transcription	Primary T cells from cord blood	blood
43	chr8:11698800-11711000	Strong transcription	Primary T helper cells fromperipheralblood	blood
44	chr8:11699000-11708800	Strong transcription	Ovary	ovary
45	chr8:11699000-11710800	Strong transcription	Primary T helper cells PMA-I stimulated	--
46	chr8:11699200-11706600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr8:11699200-11710600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr8:11699200-11710600	Strong transcription	Muscle Satellite Cultured Cells	--
49	chr8:11699400-11706600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr8:11699400-11710400	Strong transcription	Primary T cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links