Variant report

Variant	rs2652001
Chromosome Location	chr12:32192288-32192289
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	chr12:32192092..32194335-chr12:32198674..32200576,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11609494	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12227621	0.96[ASN][1000 genomes]
rs12227639	0.96[ASN][1000 genomes]
rs12296345	0.86[ASN][1000 genomes]
rs12309676	0.89[ASN][1000 genomes]
rs1260155	0.96[ASN][1000 genomes]
rs1260163	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1260166	0.96[ASN][1000 genomes]
rs1272284	0.86[ASN][1000 genomes]
rs1684125	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1684126	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1798258	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1798576	0.96[ASN][1000 genomes]
rs1798589	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1798591	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1798600	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2243419	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2388966	0.96[ASN][1000 genomes]
rs2388967	0.96[ASN][1000 genomes]
rs2594033	0.92[ASN][1000 genomes]
rs2630564	0.89[ASN][1000 genomes]
rs2630588	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2630592	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2668285	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2668287	0.80[EUR][1000 genomes]
rs2683501	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2942082	0.96[ASN][1000 genomes]
rs4442627	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs59062440	0.96[ASN][1000 genomes]
rs61926350	0.96[ASN][1000 genomes]
rs61926352	0.96[ASN][1000 genomes]
rs61926353	0.96[ASN][1000 genomes]
rs7303247	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7485882	0.96[ASN][1000 genomes]
rs901331	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs901332	1.00[ASN][1000 genomes]
rs901333	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3363806	chr12:31872264-32410283	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	esv3508621	chr12:31872654-32410593	Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	esv3508622	chr12:31872654-32410593	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	esv3430326	chr12:32142734-32216569	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	esv3410287	chr12:32142734-32219420	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv976030	chr12:32153446-32307541	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv983498	chr12:32153446-32388092	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	esv2761731	chr12:32177270-32206870	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32180200-32196200	Weak transcription	Thymus	Thymus
2	chr12:32181400-32192600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr12:32185600-32192800	Weak transcription	Fetal Heart	heart
4	chr12:32186800-32192400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr12:32186800-32192600	Weak transcription	Fetal Kidney	kidney
6	chr12:32187200-32192400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr12:32187600-32193000	Weak transcription	Fetal Intestine Large	intestine
8	chr12:32187600-32193400	Weak transcription	Fetal Intestine Small	intestine
9	chr12:32190200-32195000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr12:32190800-32193000	Enhancers	K562	blood
11	chr12:32191600-32192800	Weak transcription	Fetal Lung	lung
12	chr12:32192000-32192600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr12:32192000-32192600	Enhancers	Fetal Muscle Leg	muscle
14	chr12:32192000-32193000	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr12:32192000-32193200	Enhancers	Ovary	ovary
16	chr12:32192000-32193600	Enhancers	H1 Cell Line	embryonic stem cell
17	chr12:32192000-32193600	Enhancers	H9 Cell Line	embryonic stem cell
18	chr12:32192000-32193800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr12:32192000-32193800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr12:32192000-32193800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr12:32192000-32193800	Enhancers	Fetal Stomach	stomach
22	chr12:32192000-32194200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr12:32192200-32192400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr12:32192200-32192400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr12:32192200-32192600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr12:32192200-32192800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr12:32192200-32193000	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr12:32192200-32193400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr12:32192200-32193400	Enhancers	Placenta	Placenta
30	chr12:32192200-32193800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr12:32192200-32193800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr12:32192200-32193800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr12:32192200-32193800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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