Variant report

Variant	rs233234
Chromosome Location	chr21:45969728-45969729
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr21:45963294..45964863-chr21:45968365..45969952,2	K562	blood:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs170846	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs233235	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs233237	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs233238	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs233239	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs233240	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs233241	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs233242	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs233243	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs233244	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs233245	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs233246	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs233247	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs233248	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs233249	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35101915	0.85[EUR][1000 genomes]
rs379869	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs403603	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs439043	0.86[EUR][1000 genomes]
rs478947	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs478967	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 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	esv3361489	chr21:45669073-46013747	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	69 gene(s)	inside rSNPs	diseases
3	nsv913943	chr21:45740823-46031810	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
4	nsv913946	chr21:45838632-46031810	Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
5	nsv913948	chr21:45860912-46031810	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
6	nsv1056424	chr21:45894901-46031810	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
7	nsv544475	chr21:45894901-46031810	Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	nsv1055163	chr21:45895663-46031810	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
9	nsv459297	chr21:45941000-45989488	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv587803	chr21:45941000-45989488	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv1065798	chr21:45941000-46097463	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
12	nsv869108	chr21:45941000-46097463	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
13	nsv544476	chr21:45941000-46097463	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45967600-45970000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr21:45967600-45970800	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr21:45967600-45971000	Enhancers	H1 Cell Line	embryonic stem cell
4	chr21:45967600-45971000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr21:45967600-45971400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr21:45967600-45971800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr21:45967600-45972800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr21:45967600-45973000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr21:45967800-45969800	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr21:45967800-45969800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr21:45968000-45970800	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr21:45968000-45971200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr21:45968200-45969800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr21:45968200-45971600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr21:45968400-45969800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr21:45968400-45971400	Enhancers	HMEC	breast
17	chr21:45968400-45971600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr21:45968600-45970600	Weak transcription	Gastric	stomach
19	chr21:45968600-45970800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr21:45968800-45970400	Enhancers	Placenta	Placenta
21	chr21:45969000-45969800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr21:45969000-45971000	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr21:45969200-45969800	Enhancers	H9 Cell Line	embryonic stem cell
24	chr21:45969200-45969800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr21:45969200-45970000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr21:45969200-45971400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr21:45969400-45970400	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr21:45969400-45970600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr21:45969400-45971200	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr21:45969400-45971800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
31	chr21:45969600-45969800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr21:45969600-45969800	Enhancers	Esophagus	oesophagus
33	chr21:45969600-45969800	ZNF genes & repeats	Spleen	Spleen
34	chr21:45969600-45970800	Bivalent Enhancer	Fetal Stomach	stomach
35	chr21:45969600-45971000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr21:45969600-45971000	Enhancers	NHEK	skin
37	chr21:45969600-45971400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr21:45969600-45971600	Strong transcription	Right Atrium	heart
39	chr21:45969600-45972200	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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