Variant report

Variant	rs10218956
Chromosome Location	chr10:21965226-21965227
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	chr10:21963187..21965362-chr10:21971451..21973770,2	K562	blood:
2	chr10:21961052..21963302-chr10:21964301..21966207,2	K562	blood:

Variant related genes	Relation type
ENSG00000078403	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10047405	1.00[EUR][1000 genomes]
rs11012731	1.00[EUR][1000 genomes]
rs11012742	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12245121	1.00[EUR][1000 genomes]
rs12249032	1.00[EUR][1000 genomes]
rs12250810	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12251847	1.00[EUR][1000 genomes]
rs12260551	1.00[EUR][1000 genomes]
rs12266450	1.00[EUR][1000 genomes]
rs2183270	1.00[EUR][1000 genomes]
rs59876709	1.00[EUR][1000 genomes]
rs7068942	1.00[EUR][1000 genomes]
rs7083214	1.00[EUR][1000 genomes]
rs7904218	1.00[EUR][1000 genomes]
rs7911585	1.00[EUR][1000 genomes]
rs9971055	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036585	chr10:21833717-21998042	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv550202	chr10:21856475-22027644	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1052464	chr10:21856531-22220087	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	esv1802317	chr10:21866085-22288132	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv894947	chr10:21869609-22117913	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	esv1792771	chr10:21874152-22013644	Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
7	esv1803077	chr10:21878144-22013644	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
8	nsv550203	chr10:21916468-22062729	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21896800-21973200	Weak transcription	Hela-S3	cervix
2	chr10:21915200-21983800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr10:21915400-21967000	Weak transcription	Pancreas	Pancrea
4	chr10:21917200-21967400	Weak transcription	Brain Angular Gyrus	brain
5	chr10:21920000-21965600	Weak transcription	Esophagus	oesophagus
6	chr10:21923800-21983200	Weak transcription	NHLF	lung
7	chr10:21928600-21988200	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr10:21928800-21970200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr10:21928800-21974400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr10:21929800-21988000	Weak transcription	HUVEC	blood vessel
11	chr10:21938600-21975600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr10:21938600-21993800	Weak transcription	Lung	lung
13	chr10:21938800-21969600	Weak transcription	NHEK	skin
14	chr10:21942400-21970000	Weak transcription	HMEC	breast
15	chr10:21942400-21976200	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr10:21942400-21977400	Weak transcription	Adipose Nuclei	Adipose
17	chr10:21942400-21987200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr10:21942600-22004000	Weak transcription	NH-A	brain
19	chr10:21942800-21988400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr10:21943000-21969800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr10:21943800-22002000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr10:21945200-21976400	Weak transcription	Right Ventricle	heart
23	chr10:21951200-21989000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr10:21951800-21966000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr10:21951800-21976800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr10:21951800-21978000	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr10:21951800-21989200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr10:21952000-21975400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr10:21952000-21984800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr10:21952000-21988000	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr10:21952200-21971000	Weak transcription	Primary hematopoietic stem cells	blood
32	chr10:21952600-21983600	Weak transcription	Psoas Muscle	Psoas
33	chr10:21952800-21975800	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr10:21953000-21968200	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr10:21953200-21973000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr10:21955000-21981600	Weak transcription	Placenta	Placenta
37	chr10:21955000-21983800	Weak transcription	Stomach Smooth Muscle	stomach
38	chr10:21955000-21988000	Weak transcription	Fetal Muscle Trunk	muscle
39	chr10:21955600-21967000	Weak transcription	Small Intestine	intestine
40	chr10:21956400-21968400	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr10:21956600-21970400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr10:21956800-21988000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr10:21957000-21969800	Weak transcription	Fetal Brain Female	brain
44	chr10:21959600-21984600	Weak transcription	Colon Smooth Muscle	Colon
45	chr10:21959800-21970000	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr10:21960400-21969000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr10:21960400-21983800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr10:21961400-21981000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr10:21961400-21993800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr10:21961600-21980800	Weak transcription	Fetal Intestine Small	intestine

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