Variant report

Variant	rs35437800
Chromosome Location	chr2:21477863-21477864
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:98650231..98653086-chr2:21476515..21478101,2	MCF-7	breast:
2	chr2:21476934..21479840-chr2:21484756..21486875,2	MCF-7	breast:

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs12472945	0.81[EUR][1000 genomes]
rs13007394	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1397400	0.81[EUR][1000 genomes]
rs71437406	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7584773	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519215	chr2:21473751-21502727	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
2	nsv1011486	chr2:21475803-22364002	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv535602	chr2:21475803-22364002	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21462200-21480800	Weak transcription	Aorta	Aorta
2	chr2:21473200-21488800	Enhancers	Brain Hippocampus Middle	brain
3	chr2:21473600-21487400	Enhancers	Brain Cingulate Gyrus	brain
4	chr2:21473800-21478000	Enhancers	Brain Germinal Matrix	brain
5	chr2:21474600-21478000	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr2:21474600-21478800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:21475000-21478800	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr2:21475000-21479000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr2:21475200-21478000	Weak transcription	Adipose Nuclei	Adipose
10	chr2:21475200-21481000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr2:21475200-21484600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr2:21475800-21478800	Enhancers	Brain Substantia Nigra	brain
13	chr2:21475800-21481000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr2:21476000-21479200	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr2:21476000-21479800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:21476000-21488000	Enhancers	Brain Anterior Caudate	brain
17	chr2:21476200-21479800	Enhancers	Brain Angular Gyrus	brain
18	chr2:21476400-21479600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr2:21476400-21482000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr2:21476800-21478000	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr2:21477600-21478400	Enhancers	Spleen	Spleen
22	chr2:21477600-21479400	Enhancers	K562	blood
23	chr2:21477800-21478800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:21477800-21480200	Enhancers	Primary monocytes fromperipheralblood	blood

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