Variant report

Variant	rs535881731
Chromosome Location	chr1:186358938-186358939
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:186358800..186360589-chr1:186369488..186372003,2	MCF-7	breast:
2	chr1:186354829..186357430-chr1:186358384..186361058,3	K562	blood:
3	chr1:186344089..186347008-chr1:186357824..186359860,2	K562	blood:
4	chr1:186357371..186360885-chr1:186362480..186365023,4	K562	blood:

Variant related genes	Relation type
ENSG00000047410	Chromatin interaction
ENSG00000262180	Chromatin interaction
ENSG00000157181	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004481	chr1:186095854-186750968	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv535223	chr1:186095854-186750968	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	esv1822818	chr1:186301447-186441585	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv1012164	chr1:186323867-186565995	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	esv2762201	chr1:186323879-186566007	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv872589	chr1:186354146-186390303	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
7	esv1824284	chr1:186358588-186441585	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:186345400-186359000	Weak transcription	Lung	lung
2	chr1:186345400-186371600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:186345400-186371600	Weak transcription	Esophagus	oesophagus
4	chr1:186345400-186371600	Weak transcription	Gastric	stomach
5	chr1:186345400-186390600	Weak transcription	Small Intestine	intestine
6	chr1:186345400-186398200	Weak transcription	Spleen	Spleen
7	chr1:186345800-186361200	Weak transcription	Aorta	Aorta
8	chr1:186345800-186377400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr1:186346000-186366800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr1:186346200-186359000	Weak transcription	Brain Cingulate Gyrus	brain
11	chr1:186346200-186359000	Weak transcription	Ovary	ovary
12	chr1:186346200-186359000	Weak transcription	Thymus	Thymus
13	chr1:186346200-186360600	Weak transcription	Brain Substantia Nigra	brain
14	chr1:186346200-186361200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr1:186346200-186361200	Weak transcription	Pancreas	Pancrea
16	chr1:186346200-186361400	Weak transcription	Right Ventricle	heart
17	chr1:186346200-186365200	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr1:186346200-186365200	Weak transcription	Psoas Muscle	Psoas
19	chr1:186346200-186380400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr1:186346200-186388400	Weak transcription	Colonic Mucosa	Colon
21	chr1:186346400-186359400	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr1:186346400-186359400	Weak transcription	Colon Smooth Muscle	Colon
23	chr1:186346400-186361000	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr1:186346400-186361200	Weak transcription	Brain Angular Gyrus	brain
25	chr1:186346400-186376000	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr1:186346400-186388000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr1:186346400-186390000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr1:186346600-186359400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr1:186347200-186370800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr1:186347400-186368000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr1:186347400-186370400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
32	chr1:186347400-186370400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr1:186347600-186370800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:186348000-186359400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr1:186348000-186382000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr1:186348600-186370200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr1:186348600-186370600	Strong transcription	HUES6 Cell Line	embryonic stem cell
38	chr1:186348600-186372000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr1:186348600-186372200	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr1:186348600-186373400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:186348600-186390200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr1:186348800-186363600	Strong transcription	HUES48 Cell Line	embryonic stem cell
43	chr1:186348800-186370200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr1:186348800-186370200	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr1:186348800-186370200	Strong transcription	Dnd41	blood
46	chr1:186348800-186371000	Strong transcription	HUES64 Cell Line	embryonic stem cell
47	chr1:186348800-186372000	Strong transcription	Primary T helper cells fromperipheralblood	blood
48	chr1:186348800-186372200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr1:186349200-186368600	Strong transcription	Primary T helper cells PMA-I stimulated	--
50	chr1:186349200-186373200	Strong transcription	Monocytes-CD14+_RO01746	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links