Variant report

Variant	rs35805720
Chromosome Location	chr1:246956230-246956231
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr1:246955911-246956546	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:246947863..246950737-chr1:246955534..246958026,3	K562	blood:

Variant related genes	Relation type
KIF28P	TF binding region

Extended variants
information (count: 30 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10924825	0.84[ASN][1000 genomes]
rs12075623	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12749957	0.81[ASN][1000 genomes]
rs35853048	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3795467	0.92[ASN][1000 genomes]
rs41308152	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61852516	0.94[ASN][1000 genomes]
rs61852551	0.84[EUR][1000 genomes]
rs6667792	0.84[ASN][1000 genomes]
rs6693529	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6694274	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6703011	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7410903	0.81[ASN][1000 genomes]
rs7512440	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949571	chr1:246688635-247240863	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv873421	chr1:246818634-247044692	Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	esv2762192	chr1:246823857-247069232	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1006271	chr1:246832606-247276182	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
5	nsv535416	chr1:246832606-247276182	Strong transcription ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh 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
6	nsv430413	chr1:246845971-246975015	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
7	nsv873422	chr1:246854862-247002638	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
8	nsv1011346	chr1:246868799-247133898	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
9	nsv1006262	chr1:246892826-246964775	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
10	nsv523531	chr1:246893948-246967899	Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
11	nsv999756	chr1:246894542-246969660	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS 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	14 gene(s)	inside rSNPs	diseases
12	nsv1009436	chr1:246910373-246965832	Bivalent/Poised TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
13	nsv873423	chr1:246923861-246978504	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
14	nsv549545	chr1:246936353-246963019	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
15	nsv525154	chr1:246954166-246963019	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
16	esv3340001	chr1:246956154-246958702	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246932800-246956400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr1:246945800-246956400	Weak transcription	A549	lung
3	chr1:246946200-246956800	Weak transcription	Left Ventricle	heart
4	chr1:246949000-246957600	Weak transcription	NHDF-Ad	bronchial
5	chr1:246949400-246956800	Weak transcription	Hela-S3	cervix
6	chr1:246949400-246957600	Weak transcription	NHLF	lung
7	chr1:246952600-246956800	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr1:246952600-246957600	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr1:246952600-246957800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:246952800-246956600	Weak transcription	Placenta	Placenta
11	chr1:246952800-246956800	Weak transcription	Fetal Intestine Large	intestine
12	chr1:246952800-246957000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr1:246952800-246957000	Weak transcription	Brain Germinal Matrix	brain
14	chr1:246952800-246957600	Weak transcription	Fetal Brain Female	brain
15	chr1:246952800-246957800	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr1:246953000-246956800	Weak transcription	Fetal Brain Male	brain
17	chr1:246953000-246957600	Weak transcription	Fetal Heart	heart
18	chr1:246953000-246957600	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr1:246953000-246957600	Weak transcription	Right Ventricle	heart
20	chr1:246953000-246957800	Weak transcription	Fetal Intestine Small	intestine
21	chr1:246953200-246956800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:246953200-246957600	Weak transcription	Spleen	Spleen
23	chr1:246953400-246956400	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr1:246953400-246956400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr1:246953400-246956400	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr1:246953400-246956400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr1:246953400-246956600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:246953400-246956600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr1:246953400-246956800	Weak transcription	Fetal Muscle Leg	muscle
30	chr1:246953400-246957000	Weak transcription	Gastric	stomach
31	chr1:246953400-246957600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr1:246953400-246957600	Weak transcription	Fetal Lung	lung
33	chr1:246953400-246957600	Weak transcription	Ovary	ovary
34	chr1:246953400-246958000	Weak transcription	Fetal Kidney	kidney
35	chr1:246953400-246961600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr1:246953600-246956800	Weak transcription	Fetal Stomach	stomach
37	chr1:246954800-246957600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr1:246955600-246959400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr1:246956000-246956400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr1:246956000-246956800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr1:246956000-246957600	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr1:246956200-246957400	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr1:246956200-246959000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr1:246956200-246959200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr1:246956200-246959400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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