Variant report

Variant	rs66706635
Chromosome Location	chr2:234239735-234239736
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:234238246..234240780-chr2:234263095..234264681,2	K562	blood:
2	chr2:234237506..234239939-chr2:234241158..234243320,2	K562	blood:

Variant related genes	Relation type
ENSG00000243637	Chromatin interaction
ENSG00000077044	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10168367	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10199833	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1972906	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2304773	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28605452	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3762586	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3792104	0.87[EUR][1000 genomes]
rs3792105	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61062196	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6431282	0.87[EUR][1000 genomes]
rs73116218	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73119905	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7588509	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv584699	chr2:234182240-234255547	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv584700	chr2:234199401-234364426	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1002075	chr2:234225979-234277508	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv529419	chr2:234229606-234670426	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234223600-234245400	Weak transcription	Pancreas	Pancrea
2	chr2:234228400-234240000	Weak transcription	Fetal Intestine Small	intestine
3	chr2:234234400-234239800	Weak transcription	Thymus	Thymus
4	chr2:234237200-234242800	Enhancers	Spleen	Spleen
5	chr2:234237400-234249800	Enhancers	Primary B cells from peripheral blood	blood
6	chr2:234237800-234240000	Enhancers	Primary T cells fromperipheralblood	blood
7	chr2:234237800-234244000	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr2:234238000-234240000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr2:234238200-234240000	Enhancers	Primary B cells from cord blood	blood
10	chr2:234238200-234240000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr2:234238200-234240000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr2:234238200-234240200	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr2:234238400-234239800	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr2:234238400-234239800	Weak transcription	Fetal Thymus	thymus
15	chr2:234238400-234240000	Enhancers	Primary T cells from cord blood	blood
16	chr2:234238400-234243000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr2:234238400-234244600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr2:234238600-234239800	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr2:234238600-234239800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr2:234238600-234239800	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr2:234238600-234240000	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr2:234238600-234240000	Weak transcription	Placenta	Placenta
23	chr2:234238600-234241000	Weak transcription	Fetal Muscle Leg	muscle
24	chr2:234238800-234240000	Weak transcription	K562	blood
25	chr2:234238800-234243600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr2:234238800-234246600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr2:234239200-234243000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
28	chr2:234239400-234239800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr2:234239600-234239800	Enhancers	GM12878-XiMat	blood
30	chr2:234239600-234240200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr2:234239600-234241400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
32	chr2:234239600-234242400	Enhancers	Primary hematopoietic stem cells	blood
33	chr2:234239600-234243200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood

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