Variant report

Variant	rs67145238
Chromosome Location	chr3:140224145-140224146
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:140222088..140224189-chr3:140226256..140229076,2	K562	blood:
2	chr3:140219298..140221435-chr3:140223284..140225046,2	K562	blood:

Variant related genes	Relation type
ENSG00000250433	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12634859	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2081801	0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55776797	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs66565597	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6793607	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757891	chr3:139925764-140524730	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	esv2759181	chr3:139925764-140524730	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv527831	chr3:139932966-140533823	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv34489	chr3:140009020-140469302	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	esv2757012	chr3:140009220-140460228	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv591863	chr3:140126067-140274442	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140216400-140227600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:140218000-140227800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr3:140220200-140228000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr3:140220400-140224200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr3:140220400-140224400	Weak transcription	HSMM	muscle
6	chr3:140220800-140224200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr3:140223200-140224400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr3:140223400-140224200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr3:140223400-140224400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr3:140223400-140224600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr3:140223400-140225200	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr3:140223400-140225600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr3:140223400-140225600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr3:140223400-140225600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr3:140223400-140226200	Enhancers	HSMMtube	muscle
16	chr3:140223600-140224200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr3:140223600-140225200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:140223800-140224400	Enhancers	Brain Hippocampus Middle	brain
19	chr3:140223800-140224800	Enhancers	H9 Cell Line	embryonic stem cell
20	chr3:140223800-140225000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr3:140223800-140225000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr3:140223800-140225600	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr3:140224000-140224400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr3:140224000-140224400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr3:140224000-140224400	Enhancers	Brain Substantia Nigra	brain
26	chr3:140224000-140224400	Enhancers	Ovary	ovary
27	chr3:140224000-140225000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr3:140224000-140225000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr3:140224000-140225000	Enhancers	Fetal Muscle Leg	muscle
30	chr3:140224000-140225200	Enhancers	Adipose Nuclei	Adipose
31	chr3:140224000-140225600	Enhancers	H1 Cell Line	embryonic stem cell

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