Variant report

Variant	rs35361710
Chromosome Location	chr6:25390939-25390940
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1013045	0.85[ASN][1000 genomes]
rs1028347	0.85[ASN][1000 genomes]
rs1209305	0.85[ASN][1000 genomes]
rs12173289	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12210416	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13211247	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13217807	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1556043	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs169978	0.85[ASN][1000 genomes]
rs177333	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs215009	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs215013	0.84[ASN][1000 genomes]
rs215014	0.83[ASN][1000 genomes]
rs2690059	0.81[ASN][1000 genomes]
rs2744237	0.81[ASN][1000 genomes]
rs6456678	0.83[ASN][1000 genomes]
rs6933921	0.83[ASN][1000 genomes]
rs7760906	0.85[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	nsv883485	chr6:25259137-25437986	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv883486	chr6:25260434-25422369	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv883487	chr6:25280119-25508868	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv830612	chr6:25342408-25509758	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv601168	chr6:25346334-25393306	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	esv3433945	chr6:25389623-25391671	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25377400-25410600	Weak transcription	Gastric	stomach
2	chr6:25377800-25395600	Weak transcription	Pancreas	Pancrea
3	chr6:25383000-25403600	Weak transcription	Right Atrium	heart
4	chr6:25383600-25405000	Weak transcription	Fetal Intestine Small	intestine
5	chr6:25384200-25391600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr6:25388200-25392800	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr6:25388400-25391600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr6:25388400-25392800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:25388400-25395800	Weak transcription	Primary T cells from cord blood	blood
10	chr6:25388400-25396000	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr6:25388400-25396000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:25389000-25391000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:25389200-25392800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr6:25389400-25397400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr6:25389400-25403600	Weak transcription	Thymus	Thymus
16	chr6:25389800-25392600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr6:25390200-25391000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr6:25390200-25391600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr6:25390200-25392000	Weak transcription	Fetal Lung	lung
20	chr6:25390200-25392200	Weak transcription	Fetal Brain Male	brain
21	chr6:25390200-25392800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr6:25390200-25397400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr6:25390200-25399400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr6:25390200-25401800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr6:25390200-25405000	Weak transcription	Adipose Nuclei	Adipose
26	chr6:25390400-25392200	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr6:25390400-25392200	Weak transcription	NHDF-Ad	bronchial
28	chr6:25390400-25392600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr6:25390400-25392600	Weak transcription	NHEK	skin
30	chr6:25390400-25394200	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr6:25390400-25401600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr6:25390400-25401600	Weak transcription	HMEC	breast
33	chr6:25390800-25393000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr6:25390800-25397400	Weak transcription	Aorta	Aorta
35	chr6:25390800-25399200	Weak transcription	Fetal Thymus	thymus

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