Variant report

Variant	rs9284512
Chromosome Location	chr21:45551514-45551515
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:52)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:52 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr21:45551256-45555474	HepG2	liver:	n/a	n/a
2	EBF1	chr21:45551202-45551525	GM12878	blood:	n/a	chr21:45551344-45551357 chr21:45551345-45551356
3	POLR2A	chr21:45551268-45551969	MCF-7	breast:	n/a	n/a
4	POLR2A	chr21:45551223-45554970	PFSK-1	brain:	n/a	n/a
5	POLR2A	chr21:45551345-45553894	PANC-1	pancreas:	n/a	n/a
6	HMGN3	chr21:45551193-45551625	K562	blood:	n/a	n/a
7	USF2	chr21:45551363-45551543	Hela-S3	cervix:	n/a	n/a
8	MYC	chr21:45551487-45551815	K562	blood:	n/a	n/a
9	POLR2A	chr21:45550978-45552667	K562	blood:	n/a	n/a
10	POLR2A	chr21:45551099-45554025	MCF-7	breast:	n/a	n/a
11	POLR2A	chr21:45551276-45552073	HepG2	liver:	n/a	n/a
12	POLR2A	chr21:45550947-45553871	GM12892	blood:	n/a	n/a
13	POLR2A	chr21:45551284-45552224	ECC-1	luminal epithelium:	n/a	n/a
14	NR2F2	chr21:45550987-45551754	K562	blood:	n/a	n/a
15	ZNF263	chr21:45551108-45551922	HEK293-T-REx	kidney:	n/a	chr21:45551328-45551337 chr21:45551714-45551723
16	CCNT2	chr21:45551432-45551608	K562	blood:	n/a	n/a
17	MAX	chr21:45551491-45551730	K562	blood:	n/a	n/a
18	POLR2A	chr21:45551407-45551548	A549	lung:	n/a	n/a
19	POLR2A	chr21:45551055-45552527	GM12891	blood:	n/a	n/a
20	POLR2A	chr21:45551021-45554171	K562	blood:	n/a	n/a
21	RCOR1	chr21:45551280-45551658	K562	blood:	n/a	n/a
22	POLR2A	chr21:45550936-45556141	PFSK-1	brain:	n/a	n/a
23	POLR2A	chr21:45551090-45551957	GM12878	blood:	n/a	n/a
24	POLR2A	chr21:45551156-45552470	GM12878	blood:	n/a	n/a
25	POLR2A	chr21:45550983-45552705	GM12892	blood:	n/a	n/a
26	POLR2A	chr21:45551498-45551677	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr21:45550524-45555784	GM12878	blood:	n/a	n/a
28	POLR2A	chr21:45551426-45551565	A549	lung:	n/a	n/a
29	POLR2A	chr21:45551403-45552705	K562	blood:	n/a	n/a
30	POLR2A	chr21:45551397-45552051	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr21:45550463-45553791	K562	blood:	n/a	n/a
32	POLR2A	chr21:45550977-45554195	SK-N-MC	brain:	n/a	n/a
33	POLR2A	chr21:45551038-45552610	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr21:45551003-45552400	GM12878	blood:	n/a	n/a
35	POLR2A	chr21:45550964-45551547	GM12892	blood:	n/a	n/a
36	POLR2A	chr21:45551042-45552545	GM12891	blood:	n/a	n/a
37	POLR2A	chr21:45551043-45552467	HL-60	blood:	n/a	n/a
38	POLR2A	chr21:45551342-45551558	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr21:45551200-45552518	K562	blood:	n/a	n/a
40	POLR2A	chr21:45551006-45552761	K562	blood:	n/a	n/a
41	POLR2A	chr21:45550503-45552611	GM12892	blood:	n/a	n/a
42	MAZ	chr21:45551295-45551718	K562	blood:	n/a	n/a
43	POLR2A	chr21:45550191-45554297	K562	blood:	n/a	n/a
44	POLR2A	chr21:45550990-45552456	GM12891	blood:	n/a	n/a
45	POLR2A	chr21:45551251-45551949	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr21:45551290-45551581	A549	lung:	n/a	n/a
47	POLR2A	chr21:45551098-45552367	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr21:45551224-45552309	GM12878	blood:	n/a	n/a
49	POLR2A	chr21:45550292-45554259	K562	blood:	n/a	n/a
50	POLR2A	chr21:45551393-45551609	Raji	blood:	n/a	n/a

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45551285..45553710-chr21:45659921..45662248,2	MCF-7	breast:
2	chr21:45525797..45531105-chr21:45550576..45555096,10	MCF-7	breast:
3	chr21:45228525..45230832-chr21:45550134..45553031,3	MCF-7	breast:
4	chr21:45550802..45552649-chr21:45562821..45564566,2	MCF-7	breast:
5	chr21:45551466..45554089-chr21:45749737..45751999,2	MCF-7	breast:
6	chr21:45525708..45535025-chr21:45544493..45558414,30	MCF-7	breast:
7	chr21:45550460..45552468-chr21:45620537..45623485,2	MCF-7	breast:
8	chr21:45549496..45557767-chr21:45717764..45723476,12	K562	blood:

No data

Variant related genes	Relation type
C21orf33	TF binding region
ENSG00000255902	Chromatin interaction
ENSG00000160223	Chromatin interaction
ENSG00000241728	Chromatin interaction
ENSG00000215458	Chromatin interaction
ENSG00000160226	Chromatin interaction
ENSG00000232124	Chromatin interaction
ENSG00000184441	Chromatin interaction
ENSG00000141959	Chromatin interaction
ENSG00000241945	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1005045	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11910604	1.00[JPT][hapmap]
rs2020943	0.81[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2071144	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2071145	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2227265	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2838465	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs2838470	1.00[CEU][hapmap];0.89[JPT][hapmap];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2838479	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2838484	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2838487	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2838495	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2838497	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2838510	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs28834388	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57812760	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs57855582	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60503863	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61689295	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62226718	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62226719	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62226722	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62226723	0.92[EUR][1000 genomes]
rs62226724	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7275501	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7282644	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73909115	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8128926	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs878132	1.00[JPT][hapmap]
rs9306175	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9974767	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9975436	0.84[EUR][1000 genomes]
rs9977122	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9978109	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9978772	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9979931	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9980021	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9980063	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9982695	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.84[EUR][1000 genomes]
rs9982907	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9983551	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9983596	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 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
20	nsv533679	chr21:45551026-45768578	Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	64 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	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	chr21:45529000-45552000	Strong transcription	Duodenum Mucosa	Duodenum
14	chr21:45529000-45552000	Strong transcription	Fetal Brain Female	brain
15	chr21:45529200-45551800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr21:45529200-45551800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr21:45529200-45551800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr21:45529200-45552000	Strong transcription	Brain Germinal Matrix	brain
19	chr21:45529200-45552000	Strong transcription	Left Ventricle	heart
20	chr21:45529400-45552200	Strong transcription	Cortex derived primary cultured neurospheres	brain
21	chr21:45529600-45552000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr21:45530000-45552200	Strong transcription	Primary T helper cells PMA-I stimulated	--
23	chr21:45530600-45552600	Weak transcription	Fetal Brain Male	brain
24	chr21:45532600-45551800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr21:45532600-45552800	Weak transcription	Fetal Kidney	kidney
26	chr21:45532800-45551600	Strong transcription	Stomach Smooth Muscle	stomach
27	chr21:45533200-45552400	Strong transcription	Fetal Stomach	stomach
28	chr21:45533400-45552200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr21:45533400-45552200	Strong transcription	NHLF	lung
30	chr21:45533800-45551600	Strong transcription	Fetal Intestine Large	intestine
31	chr21:45534000-45551600	Strong transcription	H1 Cell Line	embryonic stem cell
32	chr21:45534000-45551600	Strong transcription	Thymus	Thymus
33	chr21:45534000-45551800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr21:45534000-45552000	Strong transcription	Placenta Amnion	Placenta Amnion
35	chr21:45534200-45552000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr21:45534400-45551600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
37	chr21:45534400-45551800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr21:45534600-45551800	Strong transcription	Osteobl	bone
39	chr21:45534800-45551600	Strong transcription	Primary T cells fromperipheralblood	blood
40	chr21:45535200-45552200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr21:45537000-45552000	Strong transcription	Fetal Thymus	thymus
42	chr21:45537000-45552200	Strong transcription	Right Ventricle	heart
43	chr21:45537600-45552000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
44	chr21:45539200-45553000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
45	chr21:45540600-45552000	Strong transcription	Lung	lung
46	chr21:45541000-45552800	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr21:45541200-45552800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr21:45542600-45551600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr21:45542600-45551600	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr21:45542600-45552200	Strong transcription	Primary hematopoietic stem cells short term culture	blood

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