Variant report

Variant	rs569209549
Chromosome Location	chr6:58147233-58147234
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv436517	chr6:57696174-58296165	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv3332363	chr6:57709182-58454441	Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	esv3426791	chr6:57741382-58349943	Enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	esv3440047	chr6:57766598-58396144	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	esv3372144	chr6:57908014-58519523	Strong transcription Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv435830	chr6:57912721-58515824	Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	esv3503622	chr6:57916040-58522258	Bivalent/Poised TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
8	esv3503623	chr6:57916040-58522258	Strong transcription Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
9	esv3445656	chr6:57975137-58576488	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	esv1805007	chr6:58060962-58150871	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases
11	nsv821647	chr6:58067314-58678227	Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
12	nsv869817	chr6:58071721-58614002	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
13	nsv885965	chr6:58075480-58308955	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
14	nsv523720	chr6:58075480-58770624	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
15	nsv1024377	chr6:58082084-58774716	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
16	nsv7902	chr6:58087399-58152348	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
17	nsv428148	chr6:58137660-58406917	Weak transcription Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
18	esv1810791	chr6:58139506-58148965	Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
19	esv11438	chr6:58139535-58151911	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases
20	nsv1020262	chr6:58140288-58774716	ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
21	esv2760987	chr6:58140300-58774716	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
22	nsv1029158	chr6:58142069-58759016	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
23	nsv969408	chr6:58142820-58168339	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
24	nsv830667	chr6:58143910-58258706	Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers ZNF genes & repeats	TF binding region CpG island lncRNA	4 gene(s)	inside rSNPs	diseases
25	esv3377268	chr6:58145593-58149491	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58146200-58149800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
2	chr6:58146600-58147400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr6:58146600-58147600	Bivalent/Poised TSS	HUVEC	blood vessel
4	chr6:58146600-58148000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
5	chr6:58146600-58149200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr6:58146600-58149600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
7	chr6:58146600-58149600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
8	chr6:58146600-58149800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
9	chr6:58146600-58149800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
10	chr6:58146600-58149800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
11	chr6:58146600-58149800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
12	chr6:58146800-58148200	Bivalent Enhancer	Liver	Liver
13	chr6:58146800-58149000	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:58146800-58149600	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr6:58146800-58149600	Bivalent/Poised TSS	NHDF-Ad	bronchial
16	chr6:58146800-58149600	Bivalent/Poised TSS	Osteobl	bone
17	chr6:58147000-58147400	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr6:58147000-58147400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
19	chr6:58147000-58147400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr6:58147000-58147400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr6:58147000-58147600	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr6:58147000-58147600	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:58147000-58147600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
24	chr6:58147000-58148000	Flanking Bivalent TSS/Enh	HepG2	liver
25	chr6:58147000-58148200	Bivalent/Poised TSS	NHEK	skin
26	chr6:58147000-58148400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
27	chr6:58147000-58149200	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr6:58147000-58149600	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
29	chr6:58147000-58149600	Bivalent Enhancer	Placenta	Placenta
30	chr6:58147200-58147400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr6:58147200-58147400	Bivalent/Poised TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr6:58147200-58147400	Bivalent/Poised TSS	Primary neutrophils fromperipheralblood	blood
33	chr6:58147200-58147400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr6:58147200-58147400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr6:58147200-58147400	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
36	chr6:58147200-58147400	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
37	chr6:58147200-58147400	Bivalent Enhancer	Fetal Brain Male	brain
38	chr6:58147200-58147400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr6:58147200-58147400	Bivalent Enhancer	Fetal Muscle Leg	muscle
40	chr6:58147200-58147400	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
41	chr6:58147200-58147400	Enhancers	Right Atrium	heart
42	chr6:58147200-58147400	Bivalent Enhancer	HMEC	breast
43	chr6:58147200-58147600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
44	chr6:58147200-58147600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr6:58147200-58147600	Bivalent Enhancer	Fetal Stomach	stomach
46	chr6:58147200-58147600	Bivalent Enhancer	Ovary	ovary
47	chr6:58147200-58147800	Bivalent Enhancer	Esophagus	oesophagus
48	chr6:58147200-58148200	Bivalent Enhancer	Fetal Heart	heart
49	chr6:58147200-58148200	ZNF genes & repeats	Lung	lung
50	chr6:58147200-58148200	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links