Variant report

Variant	rs57237552
Chromosome Location	chr1:9913042-9913043
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:9910251..9913174-chr1:9920173..9922421,2	K562	blood:
2	chr1:9884056..9886258-chr1:9911889..9914229,2	MCF-7	breast:
3	chr1:9910788..9913768-chr6:58778329..58780695,2	MCF-7	breast:
4	chr1:9907709..9909733-chr1:9912476..9914067,2	K562	blood:

Variant related genes	Relation type
ENSG00000171603	Chromatin interaction
ENSG00000223989	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11808614	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61785591	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61785593	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61785598	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6541067	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6659441	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6686017	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6690524	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74054125	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74054138	0.83[AMR][1000 genomes]
rs7529783	0.83[AMR][1000 genomes]
rs7536748	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7537879	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7554923	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3385337	chr1:9105242-10082223	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	549 gene(s)	inside rSNPs	diseases
2	nsv871610	chr1:9655795-10008221	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	esv3417409	chr1:9683992-10241703	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	esv3372906	chr1:9838995-10052992	Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv871146	chr1:9897001-9951288	Genic enhancers Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:9896000-9919200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr1:9896600-9913400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:9902800-9913600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:9904000-9929800	Weak transcription	Aorta	Aorta
5	chr1:9904200-9927400	Weak transcription	Colonic Mucosa	Colon
6	chr1:9904200-9927800	Weak transcription	Colon Smooth Muscle	Colon
7	chr1:9904400-9913400	Weak transcription	Fetal Lung	lung
8	chr1:9904400-9922600	Weak transcription	Pancreas	Pancrea
9	chr1:9904400-9923400	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr1:9904400-9927800	Weak transcription	Stomach Mucosa	stomach
11	chr1:9904400-9930000	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr1:9904600-9922600	Weak transcription	Ovary	ovary
13	chr1:9904600-9935000	Weak transcription	Osteobl	bone
14	chr1:9904800-9946000	Weak transcription	Fetal Kidney	kidney
15	chr1:9905200-9915400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:9906600-9927400	Weak transcription	Liver	Liver
17	chr1:9907000-9913400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr1:9907000-9919200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr1:9907000-9930000	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr1:9907400-9913600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr1:9907400-9914200	Strong transcription	Adipose Nuclei	Adipose
22	chr1:9907400-9929800	Weak transcription	Rectal Smooth Muscle	rectum
23	chr1:9908200-9913400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr1:9908200-9915000	Strong transcription	Fetal Stomach	stomach
25	chr1:9908400-9913800	Strong transcription	Esophagus	oesophagus
26	chr1:9908800-9913600	Weak transcription	Fetal Intestine Large	intestine
27	chr1:9909600-9913400	Enhancers	Fetal Brain Male	brain
28	chr1:9909800-9915000	Strong transcription	HepG2	liver
29	chr1:9910000-9913200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:9910000-9935000	Weak transcription	NHLF	lung
31	chr1:9910200-9918400	Weak transcription	Stomach Smooth Muscle	stomach
32	chr1:9910600-9913200	Enhancers	Brain Cingulate Gyrus	brain
33	chr1:9910800-9913200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr1:9910800-9913200	Enhancers	Brain Anterior Caudate	brain
35	chr1:9910800-9913600	Enhancers	Fetal Brain Female	brain
36	chr1:9910800-9913800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr1:9911000-9918400	Weak transcription	Left Ventricle	heart
38	chr1:9911000-9919600	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr1:9911000-9927400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr1:9911000-9930400	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr1:9911200-9913600	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr1:9911200-9913600	Weak transcription	Dnd41	blood
43	chr1:9911200-9932400	Weak transcription	Fetal Heart	heart
44	chr1:9911400-9913400	Weak transcription	Duodenum Mucosa	Duodenum
45	chr1:9911400-9913600	Strong transcription	Fetal Intestine Small	intestine
46	chr1:9911400-9918000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr1:9911400-9919200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr1:9911400-9919400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr1:9911400-9922600	Weak transcription	Right Ventricle	heart
50	chr1:9911400-9927200	Weak transcription	Primary T cells fromperipheralblood	blood

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