Variant report

Variant	rs35917308
Chromosome Location	chr10:89690827-89690828
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:89686969..89688514-chr10:89688807..89691753,2	K562	blood:
2	chr10:89620590..89623557-chr10:89689802..89694135,6	MCF-7	breast:
3	chr10:89685265..89687757-chr10:89688407..89691640,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000171862	Chromatin interaction
ENSG00000227268	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs17849092	1.00[GIH][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1793518	chr10:89625582-89733420	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	esv1798260	chr10:89625582-89733420	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv1044043	chr10:89678935-89701069	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv1794722	chr10:89690827-89725294	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	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:89647000-89711200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr10:89663800-89725400	Weak transcription	Colonic Mucosa	Colon
3	chr10:89666000-89712400	Weak transcription	Fetal Brain Male	brain
4	chr10:89673600-89726000	Weak transcription	Brain Substantia Nigra	brain
5	chr10:89674200-89695200	Weak transcription	Brain Cingulate Gyrus	brain
6	chr10:89674200-89711000	Weak transcription	HepG2	liver
7	chr10:89674600-89695600	Weak transcription	Fetal Muscle Trunk	muscle
8	chr10:89674800-89724400	Weak transcription	Fetal Brain Female	brain
9	chr10:89675400-89726000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr10:89675600-89705000	Weak transcription	Fetal Stomach	stomach
11	chr10:89675600-89705200	Weak transcription	Esophagus	oesophagus
12	chr10:89676600-89695400	Weak transcription	Brain Anterior Caudate	brain
13	chr10:89676800-89691000	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr10:89678000-89694200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr10:89679800-89691600	Weak transcription	Brain Hippocampus Middle	brain
16	chr10:89681800-89691200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr10:89682000-89705200	Weak transcription	Fetal Intestine Small	intestine
18	chr10:89682000-89705200	Weak transcription	Left Ventricle	heart
19	chr10:89682000-89705600	Weak transcription	Lung	lung
20	chr10:89682400-89705200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr10:89683200-89695600	Weak transcription	Fetal Muscle Leg	muscle
22	chr10:89683200-89705000	Weak transcription	Thymus	Thymus
23	chr10:89683200-89715200	Weak transcription	Pancreas	Pancrea
24	chr10:89683200-89720800	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr10:89683200-89723800	Weak transcription	Psoas Muscle	Psoas
26	chr10:89684000-89707400	Strong transcription	Dnd41	blood
27	chr10:89684000-89725600	Weak transcription	Gastric	stomach
28	chr10:89684000-89726200	Weak transcription	Spleen	Spleen
29	chr10:89684800-89702200	Weak transcription	Fetal Kidney	kidney
30	chr10:89685400-89692200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr10:89685800-89712400	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr10:89686400-89691800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr10:89686400-89692800	Weak transcription	Placenta	Placenta
34	chr10:89686400-89693200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr10:89686600-89691200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr10:89686600-89692400	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr10:89686600-89692800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr10:89686600-89695600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr10:89686600-89698800	Weak transcription	K562	blood
40	chr10:89686600-89711200	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr10:89686800-89708400	Weak transcription	Aorta	Aorta
42	chr10:89686800-89710400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr10:89687000-89691200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr10:89687000-89691200	Enhancers	Liver	Liver
45	chr10:89687000-89712200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr10:89687200-89691200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr10:89687200-89692600	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr10:89687200-89694000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr10:89687200-89705800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr10:89687200-89705800	Weak transcription	Small Intestine	intestine

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