Variant report

Variant	rs2187313
Chromosome Location	chr21:45544594-45544595
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr21:45544320-45544727	K562	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr21:45538834..45541365-chr21:45544290..45547592,5	MCF-7	breast:
2	chr21:45538845..45541802-chr21:45543928..45546448,4	MCF-7	breast:
3	chr21:45525708..45535025-chr21:45544493..45558414,30	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ICOSLG-10	chr21:45544588-45544882	NONHSAT082473

No data

Variant related genes	Relation type
PWP2	TF binding region
ENSG00000241945	Chromatin interaction

Extended variants
information (count: 146 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:127)

rs_ID	r²[population]
rs1051981	0.93[ASW][hapmap];0.89[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[TSI][hapmap];0.88[YRI][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1059813	0.88[EUR][1000 genomes]
rs11089111	0.87[EUR][1000 genomes]
rs11089115	0.89[CEU][hapmap]
rs11700840	0.81[EUR][1000 genomes]
rs11700919	0.87[EUR][1000 genomes]
rs12627239	0.83[CEU][hapmap];0.85[EUR][1000 genomes]
rs13046297	0.89[CEU][hapmap]
rs13047030	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13048551	0.81[EUR][1000 genomes]
rs13048791	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs17004630	1.00[CHB][hapmap];0.89[CHD][hapmap];0.85[GIH][hapmap];0.92[JPT][hapmap]
rs1858665	0.89[CEU][hapmap];0.88[EUR][1000 genomes]
rs2006694	1.00[CHB][hapmap];0.85[JPT][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2020945	0.84[CEU][hapmap];0.94[TSI][hapmap];0.87[EUR][1000 genomes]
rs2020946	0.83[CEU][hapmap];0.87[EUR][1000 genomes]
rs2039272	0.85[EUR][1000 genomes]
rs2051260	0.87[EUR][1000 genomes]
rs2071135	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2071142	0.84[CEU][hapmap];0.94[TSI][hapmap];0.89[EUR][1000 genomes]
rs2071143	0.84[CEU][hapmap];0.97[TSI][hapmap];0.88[EUR][1000 genomes]
rs2071146	0.89[CEU][hapmap];0.88[EUR][1000 genomes]
rs2071147	0.88[EUR][1000 genomes]
rs2071154	0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap];0.85[YRI][hapmap];0.85[ASN][1000 genomes]
rs2073432	0.89[CEU][hapmap];0.87[EUR][1000 genomes]
rs2073433	0.89[CEU][hapmap];0.88[EUR][1000 genomes]
rs2073435	0.89[EUR][1000 genomes]
rs2238711	0.81[TSI][hapmap]
rs2238713	0.88[EUR][1000 genomes]
rs2242950	0.89[CEU][hapmap];0.85[EUR][1000 genomes]
rs2242951	1.00[ASN][1000 genomes]
rs2242953	0.89[CEU][hapmap];0.89[EUR][1000 genomes]
rs2242954	0.89[CEU][hapmap];0.85[EUR][1000 genomes]
rs2243999	0.84[CEU][hapmap];0.94[TSI][hapmap];0.87[EUR][1000 genomes]
rs2245462	0.81[TSI][hapmap]
rs2251267	0.89[CEU][hapmap];0.97[TSI][hapmap];0.88[EUR][1000 genomes]
rs2255016	0.80[ASN][1000 genomes]
rs2255828	0.83[CEU][hapmap];0.81[MEX][hapmap];0.85[TSI][hapmap]
rs2255955	0.94[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2276530	0.83[CEU][hapmap]
rs2276532	0.90[CHB][hapmap];0.92[JPT][hapmap]
rs2277805	0.86[ASW][hapmap];0.89[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.80[YRI][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2277806	0.84[CEU][hapmap];0.94[TSI][hapmap];0.84[EUR][1000 genomes]
rs2299815	0.83[CEU][hapmap]
rs2299816	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs2299817	0.90[CHB][hapmap];0.96[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap]
rs2329707	0.88[EUR][1000 genomes]
rs2516519	0.87[EUR][1000 genomes]
rs2516521	0.88[EUR][1000 genomes]
rs2776368	0.87[EUR][1000 genomes]
rs2838464	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs2838469	0.94[CEU][hapmap];0.90[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.87[TSI][hapmap];0.81[EUR][1000 genomes]
rs2838471	0.81[EUR][1000 genomes]
rs2838473	0.83[CEU][hapmap]
rs2838482	0.83[CEU][hapmap]
rs2838486	0.84[CEU][hapmap];0.85[TSI][hapmap]
rs2838488	0.85[EUR][1000 genomes]
rs2838489	0.88[EUR][1000 genomes]
rs2838490	0.89[CEU][hapmap];0.94[TSI][hapmap];0.89[EUR][1000 genomes]
rs2838491	0.89[CEU][hapmap];0.97[TSI][hapmap];0.88[EUR][1000 genomes]
rs2838492	0.88[CEU][hapmap];0.88[EUR][1000 genomes]
rs2838493	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2838494	0.89[CEU][hapmap];0.86[EUR][1000 genomes]
rs2838496	0.89[CEU][hapmap];0.87[EUR][1000 genomes]
rs2838498	0.86[EUR][1000 genomes]
rs2838499	0.87[EUR][1000 genomes]
rs2838502	0.84[CEU][hapmap];0.94[TSI][hapmap];0.81[EUR][1000 genomes]
rs2838503	0.89[CEU][hapmap];0.91[TSI][hapmap]
rs2838507	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs2838508	0.81[CHB][hapmap];0.93[CHD][hapmap];0.92[GIH][hapmap];0.85[JPT][hapmap];0.91[TSI][hapmap]
rs2838509	1.00[CHB][hapmap];0.93[CHD][hapmap];0.92[GIH][hapmap];0.85[JPT][hapmap];0.90[TSI][hapmap]
rs2850150	0.85[EUR][1000 genomes]
rs2850154	0.93[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2850155	0.87[EUR][1000 genomes]
rs2850156	0.89[EUR][1000 genomes]
rs2850157	0.89[EUR][1000 genomes]
rs2855651	0.88[EUR][1000 genomes]
rs2855652	0.89[EUR][1000 genomes]
rs2855653	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35524612	0.93[ASN][1000 genomes]
rs35538274	0.86[EUR][1000 genomes]
rs3788104	1.00[CHB][hapmap];0.92[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3788108	1.00[CHB][hapmap];0.93[JPT][hapmap];0.89[YRI][hapmap];0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4818881	0.89[CEU][hapmap];0.87[EUR][1000 genomes]
rs4818886	1.00[CHB][hapmap];0.89[CHD][hapmap]
rs4819361	0.81[CHB][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap]
rs4819362	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs4819370	0.83[EUR][1000 genomes]
rs4819372	0.82[EUR][1000 genomes]
rs4819373	0.87[EUR][1000 genomes]
rs4819375	1.00[CHB][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs4819376	0.89[CEU][hapmap];0.94[TSI][hapmap];0.89[EUR][1000 genomes]
rs4819377	0.88[EUR][1000 genomes]
rs4819378	0.89[CEU][hapmap];0.86[EUR][1000 genomes]
rs4819379	0.87[EUR][1000 genomes]
rs4819380	0.98[ASN][1000 genomes]
rs4819381	0.86[EUR][1000 genomes]
rs4819383	0.89[CEU][hapmap]
rs59675192	0.81[ASN][1000 genomes]
rs62226688	0.92[ASN][1000 genomes]
rs7277269	0.90[TSI][hapmap];0.83[EUR][1000 genomes]
rs7279319	0.81[EUR][1000 genomes]
rs7280558	0.91[TSI][hapmap]
rs7280581	0.88[EUR][1000 genomes]
rs7281270	0.85[EUR][1000 genomes]
rs7281291	0.81[EUR][1000 genomes]
rs7281768	0.82[CEU][hapmap]
rs7282324	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs756553	0.89[EUR][1000 genomes]
rs756554	0.89[CEU][hapmap];0.97[TSI][hapmap];0.87[EUR][1000 genomes]
rs756555	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs7676	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.92[YRI][hapmap];0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8126564	0.86[EUR][1000 genomes]
rs8130647	0.88[EUR][1000 genomes]
rs8132918	0.84[EUR][1000 genomes]
rs8133610	0.83[EUR][1000 genomes]
rs885872	1.00[ASW][hapmap];0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs915774	0.85[TSI][hapmap]
rs9306171	0.81[TSI][hapmap]
rs9306172	0.84[CEU][hapmap];0.90[TSI][hapmap]
rs965733	0.90[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs9680179	0.85[EUR][1000 genomes]
rs968713	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs968714	0.89[CEU][hapmap];0.97[TSI][hapmap];0.88[EUR][1000 genomes]
rs9977564	0.81[EUR][1000 genomes]
rs9981485	0.81[EUR][1000 genomes]
rs9985064	1.00[CHB][hapmap];0.85[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33817	chr21:45169412-46031810	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
2	nsv913887	chr21:45344799-45670770	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv459293	chr21:45415913-45555079	Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv587721	chr21:45415913-45555079	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv1064420	chr21:45460089-45814986	Enhancers Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
6	nsv544472	chr21:45460089-45814986	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
7	nsv432155	chr21:45479055-45772388	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
8	nsv913890	chr21:45482950-45603746	Genic enhancers Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
9	nsv459294	chr21:45499171-45595060	Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Weak transcription Bivalent Enhancer 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 target site	32 gene(s)	inside rSNPs	diseases
10	nsv587722	chr21:45499171-45595060	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
11	nsv913891	chr21:45508561-45588518	Strong transcription Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
12	nsv913892	chr21:45508561-45595060	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers 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	32 gene(s)	inside rSNPs	diseases
13	nsv913893	chr21:45508561-45603746	Flanking Active TSS Strong transcription Genic enhancers Active TSS Enhancers Weak transcription Bivalent Enhancer 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 target site	32 gene(s)	inside rSNPs	diseases
14	nsv913894	chr21:45508561-45627976	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
15	nsv913895	chr21:45528919-45595060	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer 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 miRNA target site	31 gene(s)	inside rSNPs	diseases
16	nsv913896	chr21:45528919-45603746	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
17	nsv913897	chr21:45528919-45640139	Strong transcription Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
18	esv1825445	chr21:45535566-45754936	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
19	esv1817474	chr21:45540607-45773102	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2187313	PWP2	cis	lymphoblastoid	seeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45528200-45552800	Weak transcription	Right Atrium	heart
2	chr21:45528600-45551800	Strong transcription	HUES6 Cell Line	embryonic stem cell
3	chr21:45528800-45551800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr21:45528800-45551800	Strong transcription	HUES48 Cell Line	embryonic stem cell
5	chr21:45528800-45552000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr21:45528800-45552000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr21:45528800-45552000	Strong transcription	Rectal Mucosa Donor 29	rectum
8	chr21:45528800-45552200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr21:45528800-45552200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr21:45528800-45552400	Weak transcription	Fetal Heart	heart
11	chr21:45528800-45552400	Strong transcription	Fetal Intestine Small	intestine
12	chr21:45528800-45552600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr21:45529000-45547200	Strong transcription	Liver	Liver
14	chr21:45529000-45549200	Strong transcription	HepG2	liver
15	chr21:45529000-45549400	Strong transcription	HMEC	breast
16	chr21:45529000-45551000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr21:45529000-45551200	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr21:45529000-45552000	Strong transcription	Duodenum Mucosa	Duodenum
19	chr21:45529000-45552000	Strong transcription	Fetal Brain Female	brain
20	chr21:45529200-45551200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr21:45529200-45551200	Strong transcription	Sigmoid Colon	Sigmoid Colon
22	chr21:45529200-45551400	Strong transcription	Ovary	ovary
23	chr21:45529200-45551800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr21:45529200-45551800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr21:45529200-45551800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr21:45529200-45552000	Strong transcription	Brain Germinal Matrix	brain
27	chr21:45529200-45552000	Strong transcription	Left Ventricle	heart
28	chr21:45529400-45551000	Strong transcription	Primary T cells from cord blood	blood
29	chr21:45529400-45551200	Strong transcription	Muscle Satellite Cultured Cells	--
30	chr21:45529400-45551400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr21:45529400-45552200	Strong transcription	Cortex derived primary cultured neurospheres	brain
32	chr21:45529600-45552000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr21:45530000-45551400	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr21:45530000-45552200	Strong transcription	Primary T helper cells PMA-I stimulated	--
35	chr21:45530200-45550800	Strong transcription	Dnd41	blood
36	chr21:45530600-45552600	Weak transcription	Fetal Brain Male	brain
37	chr21:45532000-45551200	Strong transcription	Pancreas	Pancrea
38	chr21:45532000-45551200	Strong transcription	Skeletal Muscle Female	skeletal muscle
39	chr21:45532400-45551400	Strong transcription	Colonic Mucosa	Colon
40	chr21:45532600-45551800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr21:45532600-45552800	Weak transcription	Fetal Kidney	kidney
42	chr21:45532800-45551600	Strong transcription	Stomach Smooth Muscle	stomach
43	chr21:45533200-45552400	Strong transcription	Fetal Stomach	stomach
44	chr21:45533400-45552200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr21:45533400-45552200	Strong transcription	NHLF	lung
46	chr21:45533600-45548800	Strong transcription	Rectal Mucosa Donor 31	rectum
47	chr21:45533800-45545000	Strong transcription	Brain Substantia Nigra	brain
48	chr21:45533800-45546600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr21:45533800-45551400	Strong transcription	H9 Cell Line	embryonic stem cell
50	chr21:45533800-45551600	Strong transcription	Fetal Intestine Large	intestine

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