Variant report

Variant	rs2503826
Chromosome Location	chr6:5411645-5411646
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1364554	1.00[EUR][1000 genomes]
rs1469191	1.00[EUR][1000 genomes]
rs1469192	1.00[EUR][1000 genomes]
rs1549362	1.00[EUR][1000 genomes]
rs2113693	1.00[MEX][hapmap];1.00[EUR][1000 genomes]
rs2432751	1.00[EUR][1000 genomes]
rs2432759	1.00[EUR][1000 genomes]
rs2432782	1.00[EUR][1000 genomes]
rs2432787	1.00[EUR][1000 genomes]
rs2503807	1.00[EUR][1000 genomes]
rs2503810	1.00[EUR][1000 genomes]
rs58896310	1.00[EUR][1000 genomes]
rs9504387	1.00[EUR][1000 genomes]
rs9504395	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031837	chr6:4996667-5418726	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
2	nsv1030254	chr6:5132261-5431585	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1019428	chr6:5216835-5627839	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv538118	chr6:5216835-5627839	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv830578	chr6:5264086-5455570	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1022738	chr6:5298362-5411645	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv883417	chr6:5307432-5431340	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv883418	chr6:5307432-5501389	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv1015643	chr6:5311590-5452427	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1034607	chr6:5311590-5573514	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv538120	chr6:5311590-5573514	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv916361	chr6:5315853-5695486	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv1030744	chr6:5328012-5458222	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv1023027	chr6:5377308-5556749	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
15	nsv538121	chr6:5377308-5556749	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
16	nsv1022505	chr6:5388025-5449240	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
17	nsv5180	chr6:5389197-5434354	Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5369400-5419800	Weak transcription	Aorta	Aorta
2	chr6:5369600-5417400	Weak transcription	Fetal Intestine Small	intestine
3	chr6:5374400-5431400	Weak transcription	Primary B cells from cord blood	blood
4	chr6:5395400-5431200	Weak transcription	Left Ventricle	heart
5	chr6:5399200-5415800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:5399200-5440000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr6:5403200-5412200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:5403200-5439800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr6:5403400-5412400	Weak transcription	Brain Substantia Nigra	brain
10	chr6:5403400-5445200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr6:5403600-5411800	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr6:5403600-5412400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr6:5403600-5418600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr6:5403600-5437600	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr6:5404200-5419800	Weak transcription	Dnd41	blood
16	chr6:5404400-5412400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr6:5404400-5412600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr6:5404400-5412600	Weak transcription	HMEC	breast
19	chr6:5404600-5412400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr6:5404800-5428200	Weak transcription	Lung	lung
21	chr6:5405200-5431000	Weak transcription	Duodenum Mucosa	Duodenum
22	chr6:5405400-5439800	Weak transcription	Pancreas	Pancrea
23	chr6:5406600-5412200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr6:5406600-5431400	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr6:5406800-5417600	Weak transcription	Primary hematopoietic stem cells	blood
26	chr6:5407000-5415800	Weak transcription	Fetal Stomach	stomach
27	chr6:5407000-5431000	Weak transcription	Primary B cells from peripheral blood	blood
28	chr6:5407400-5439600	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr6:5408200-5417800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr6:5408400-5413000	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr6:5408600-5412400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr6:5408600-5431200	Weak transcription	Gastric	stomach
33	chr6:5409200-5412000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr6:5410200-5431200	Weak transcription	Primary T cells fromperipheralblood	blood
35	chr6:5410400-5427600	Weak transcription	Thymus	Thymus
36	chr6:5410800-5421200	Weak transcription	Primary T cells from cord blood	blood
37	chr6:5411200-5413800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr6:5411400-5411800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr6:5411400-5412800	Enhancers	H1 Cell Line	embryonic stem cell
40	chr6:5411400-5412800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr6:5411400-5412800	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr6:5411600-5412000	Weak transcription	Ovary	ovary
43	chr6:5411600-5413200	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr6:5411600-5413600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr6:5411600-5413800	Weak transcription	Psoas Muscle	Psoas
46	chr6:5411600-5431200	Weak transcription	HepG2	liver
47	chr6:5411600-5432800	Weak transcription	Fetal Muscle Leg	muscle

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