Variant report

Variant	rs3845410
Chromosome Location	chr1:180879415-180879416
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	chr1:180873512..180876781-chr1:180876890..180880881,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA1614-1	chr1:180878158-180879637	NONHSAT008270

Variant related genes	Relation type
ENSG00000225857	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs16856482	0.82[EUR][1000 genomes]
rs3845409	0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs41268446	0.82[EUR][1000 genomes]
rs4382679	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4652537	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61811250	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014404	chr1:180770155-181090200	Weak transcription Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	97 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:180805800-180881000	Weak transcription	Aorta	Aorta
2	chr1:180824000-180880800	Weak transcription	Right Ventricle	heart
3	chr1:180861200-180880800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr1:180868800-180880400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr1:180868800-180881000	Weak transcription	Right Atrium	heart
6	chr1:180869600-180881000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:180869800-180880800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr1:180870800-180880600	Weak transcription	Brain Germinal Matrix	brain
9	chr1:180875000-180879800	Weak transcription	Colon Smooth Muscle	Colon
10	chr1:180877600-180881200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr1:180878400-180880400	Enhancers	Fetal Lung	lung
12	chr1:180878400-180881000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr1:180878600-180881000	Weak transcription	Lung	lung
14	chr1:180879000-180879800	Weak transcription	Fetal Thymus	thymus
15	chr1:180879000-180880800	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr1:180879000-180881000	Enhancers	Fetal Heart	heart
17	chr1:180879200-180880000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr1:180879200-180880000	Enhancers	GM12878-XiMat	blood
19	chr1:180879200-180880400	Enhancers	Stomach Smooth Muscle	stomach
20	chr1:180879200-180880600	Weak transcription	Fetal Kidney	kidney
21	chr1:180879200-180881800	Weak transcription	A549	lung
22	chr1:180879400-180879600	Weak transcription	Fetal Muscle Leg	muscle
23	chr1:180879400-180880400	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr1:180879400-180880600	Weak transcription	Fetal Brain Male	brain
25	chr1:180879400-180880800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr1:180879400-180880800	Enhancers	Fetal Stomach	stomach
27	chr1:180879400-180881000	Enhancers	Left Ventricle	heart

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