Variant report

Variant	rs4931013
Chromosome Location	chr12:32560722-32560723
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BICD1-3	chr12:32560576-32560852	NONHSAT027612

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1055876	0.83[ASN][1000 genomes]
rs11051969	0.83[ASN][1000 genomes]
rs11051973	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11051975	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11051976	0.89[ASN][1000 genomes]
rs11051985	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11051986	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11051987	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11051988	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11051989	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11051991	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11051992	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11052002	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12227991	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12228004	0.84[ASN][1000 genomes]
rs12229856	0.83[ASN][1000 genomes]
rs2728683	0.80[EUR][1000 genomes]
rs2728684	0.81[EUR][1000 genomes]
rs2728709	0.89[EUR][1000 genomes]
rs4931623	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56670459	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6488050	0.83[ASN][1000 genomes]
rs7132235	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7297381	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73084099	0.84[ASN][1000 genomes]
rs73084101	0.91[ASN][1000 genomes]
rs73086036	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73086040	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73088096	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7309706	0.84[ASN][1000 genomes]
rs7313432	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531960	chr12:32257285-32775277	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	esv2751096	chr12:32280340-32702784	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv469346	chr12:32531220-32587465	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv558188	chr12:32531220-32587465	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1054191	chr12:32534619-32733066	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv541455	chr12:32534619-32733066	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	esv3342938	chr12:32551041-32716745	Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv469347	chr12:32555846-32602079	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv558189	chr12:32555846-32602079	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32553400-32572200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:32553400-32572200	Weak transcription	HSMMtube	muscle
3	chr12:32553400-32572400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:32553600-32572600	Weak transcription	Esophagus	oesophagus
5	chr12:32553800-32571600	Weak transcription	Left Ventricle	heart
6	chr12:32554000-32572200	Weak transcription	Right Ventricle	heart
7	chr12:32554200-32561200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr12:32554200-32566400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr12:32554200-32571800	Weak transcription	Ovary	ovary
10	chr12:32554200-32573800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr12:32554600-32572400	Weak transcription	Fetal Intestine Large	intestine
12	chr12:32554600-32593200	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr12:32555400-32571400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr12:32555400-32572000	Weak transcription	Duodenum Mucosa	Duodenum
15	chr12:32555600-32571400	Weak transcription	Lung	lung
16	chr12:32556000-32571800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr12:32556200-32561600	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr12:32556400-32561600	Weak transcription	Fetal Intestine Small	intestine
19	chr12:32556400-32562600	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr12:32556400-32571600	Weak transcription	HMEC	breast
21	chr12:32556600-32561400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr12:32557000-32561400	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr12:32557000-32563400	Weak transcription	Pancreas	Pancrea
24	chr12:32557200-32561400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr12:32557400-32561600	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr12:32557400-32571200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr12:32557600-32561200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:32557600-32561600	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr12:32557600-32563200	Weak transcription	NHEK	skin
30	chr12:32558600-32561400	Weak transcription	Stomach Mucosa	stomach
31	chr12:32558800-32562800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr12:32558800-32566400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr12:32559200-32561400	Weak transcription	Gastric	stomach
34	chr12:32559200-32571200	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr12:32559600-32566400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr12:32559800-32572400	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr12:32560200-32563800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr12:32560400-32561800	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr12:32560600-32571400	Weak transcription	H9 Cell Line	embryonic stem cell

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