Variant report

Variant	rs10178563
Chromosome Location	chr2:173353856-173353857
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:173352292..173355193-chr2:173355588..173357472,2	K562	blood:
2	chr2:173352359..173353981-chr2:173354286..173356904,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000091409	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10167416	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10195845	0.92[YRI][hapmap]
rs10209072	1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10209090	0.93[YRI][hapmap]
rs10221599	0.84[YRI][hapmap]
rs13389355	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13426548	0.93[YRI][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533927	chr2:173161637-173796894	Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer 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	44 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173321400-173356000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:173327800-173370800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:173329800-173371200	Weak transcription	Hela-S3	cervix
4	chr2:173330400-173360400	Weak transcription	Small Intestine	intestine
5	chr2:173330600-173371400	Strong transcription	HUES64 Cell Line	embryonic stem cell
6	chr2:173330600-173372200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr2:173330600-173373200	Strong transcription	NHEK	skin
8	chr2:173330600-173373400	Strong transcription	HUES48 Cell Line	embryonic stem cell
9	chr2:173330600-173373400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr2:173330600-173373600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr2:173330600-173374200	Weak transcription	Stomach Mucosa	stomach
12	chr2:173331000-173370000	Strong transcription	Rectal Mucosa Donor 29	rectum
13	chr2:173331000-173373200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr2:173331000-173373400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr2:173331000-173373800	Strong transcription	HMEC	breast
16	chr2:173331200-173372000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
17	chr2:173331400-173370200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr2:173335400-173354000	Strong transcription	Primary neutrophils fromperipheralblood	blood
19	chr2:173337800-173360200	Strong transcription	Fetal Thymus	thymus
20	chr2:173343000-173360200	Strong transcription	Sigmoid Colon	Sigmoid Colon
21	chr2:173344000-173356000	Weak transcription	Fetal Kidney	kidney
22	chr2:173345800-173359800	Weak transcription	Placenta	Placenta
23	chr2:173345800-173360800	Strong transcription	Duodenum Mucosa	Duodenum
24	chr2:173346000-173354200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr2:173346000-173360800	Strong transcription	HSMM	muscle
26	chr2:173346000-173370200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr2:173346000-173370200	Strong transcription	HUES6 Cell Line	embryonic stem cell
28	chr2:173346000-173370600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr2:173346400-173354000	Strong transcription	Fetal Intestine Small	intestine
30	chr2:173346400-173356000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr2:173346400-173371400	Weak transcription	NHLF	lung
32	chr2:173346600-173356000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr2:173346600-173356000	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr2:173346600-173357600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr2:173346800-173356000	Weak transcription	Brain Cingulate Gyrus	brain
36	chr2:173347000-173367200	Strong transcription	Cortex derived primary cultured neurospheres	brain
37	chr2:173347400-173368600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr2:173347800-173371600	Weak transcription	Fetal Brain Male	brain
39	chr2:173347800-173376200	Weak transcription	Fetal Heart	heart
40	chr2:173349200-173356800	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr2:173349200-173357400	Strong transcription	Skeletal Muscle Female	skeletal muscle
42	chr2:173349200-173358000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr2:173349400-173360200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr2:173349400-173360200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr2:173349400-173360800	Strong transcription	Fetal Intestine Large	intestine
46	chr2:173349400-173365200	Strong transcription	H1 Cell Line	embryonic stem cell
47	chr2:173349400-173370400	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr2:173349600-173354000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr2:173349600-173356000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr2:173349800-173354000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood

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