Variant report

Variant	rs7290420
Chromosome Location	chr22:30136137-30136138
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr22:30133945..30136337-chr22:30161656..30163853,2	MCF-7	breast:
2	chr22:30135111..30137455-chr22:30141470..30144208,2	K562	blood:
3	chr22:30136102..30138464-chr22:30143800..30146252,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000184076	Chromatin interaction
ENSG00000100319	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1001318	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1071962	0.90[GIH][hapmap]
rs12158466	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs12159277	1.00[CEU][hapmap]
rs12159536	1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12163073	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12627866	1.00[CEU][hapmap];0.90[GIH][hapmap]
rs12628545	1.00[CEU][hapmap]
rs13057811	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.93[MKK][hapmap];0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs14115	1.00[CEU][hapmap];0.90[GIH][hapmap];0.84[TSI][hapmap];0.82[EUR][1000 genomes]
rs16988049	1.00[CEU][hapmap]
rs17711461	0.90[GIH][hapmap]
rs17711508	0.90[GIH][hapmap]
rs2018808	0.82[EUR][1000 genomes]
rs2232903	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2240365	1.00[CEU][hapmap]
rs2240366	0.90[GIH][hapmap];0.84[TSI][hapmap]
rs28730892	0.82[EUR][1000 genomes]
rs5997507	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs5997508	1.00[ASN][1000 genomes]
rs5997509	0.90[AFR][1000 genomes]
rs5997515	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs5997518	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs5997519	0.82[EUR][1000 genomes]
rs5997520	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs5997524	0.82[EUR][1000 genomes]
rs6006234	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6006235	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6006238	1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6006239	1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6006241	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6006247	0.82[EUR][1000 genomes]
rs6006249	0.82[EUR][1000 genomes]
rs6006250	0.82[EUR][1000 genomes]
rs6006262	0.82[EUR][1000 genomes]
rs60102307	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs71331211	1.00[ASN][1000 genomes]
rs7285660	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs7285800	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs73394838	0.82[EUR][1000 genomes]
rs740116	1.00[CEU][hapmap];0.90[GIH][hapmap]
rs8138165	0.82[EUR][1000 genomes]

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	nsv529742	chr22:29677909-30274388	Bivalent Enhancer Enhancers ZNF genes & repeats Strong transcription Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1064081	chr22:29826745-30623965	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv544677	chr22:29826745-30623965	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	nsv914964	chr22:30081715-30150549	Bivalent Enhancer Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv515720	chr22:30081715-30163526	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv914966	chr22:30088442-30138548	Weak transcription Bivalent Enhancer Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv1065072	chr22:30102176-30155245	Strong transcription Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30117000-30137200	Weak transcription	HSMM	muscle
2	chr22:30123200-30137600	Weak transcription	Osteobl	bone
3	chr22:30123200-30142800	Weak transcription	Brain Substantia Nigra	brain
4	chr22:30123600-30146800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr22:30123600-30147000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr22:30123800-30136600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr22:30124600-30136600	Weak transcription	Primary B cells from cord blood	blood
8	chr22:30125400-30146200	Weak transcription	NHLF	lung
9	chr22:30126000-30144600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr22:30126600-30145200	Strong transcription	Primary T cells from cord blood	blood
11	chr22:30127600-30140600	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr22:30127800-30137200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr22:30128200-30136200	Weak transcription	Small Intestine	intestine
14	chr22:30129000-30139200	Strong transcription	Stomach Smooth Muscle	stomach
15	chr22:30129400-30139000	Strong transcription	Primary T helper cells fromperipheralblood	blood
16	chr22:30129400-30144600	Strong transcription	Liver	Liver
17	chr22:30129800-30138600	Strong transcription	Left Ventricle	heart
18	chr22:30129800-30141000	Strong transcription	Fetal Stomach	stomach
19	chr22:30130000-30141000	Weak transcription	Colon Smooth Muscle	Colon
20	chr22:30130200-30150200	Weak transcription	A549	lung
21	chr22:30130400-30150600	Strong transcription	Fetal Intestine Small	intestine
22	chr22:30130600-30140200	Strong transcription	Skeletal Muscle Male	skeletal muscle
23	chr22:30130600-30149800	Weak transcription	Psoas Muscle	Psoas
24	chr22:30130800-30138000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr22:30130800-30138800	Strong transcription	Spleen	Spleen
26	chr22:30130800-30139200	Weak transcription	NH-A	brain
27	chr22:30131000-30138800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr22:30131000-30145800	Weak transcription	Primary hematopoietic stem cells	blood
29	chr22:30131200-30139800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr22:30131400-30148600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr22:30131600-30136400	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr22:30131600-30136400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr22:30131600-30137200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr22:30131600-30142200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr22:30131600-30144800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr22:30131600-30145600	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr22:30131600-30162000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr22:30131800-30138800	Strong transcription	Brain Germinal Matrix	brain
39	chr22:30131800-30138800	Strong transcription	Duodenum Smooth Muscle	Duodenum
40	chr22:30131800-30147200	Strong transcription	Brain Inferior Temporal Lobe	brain
41	chr22:30132800-30138800	Strong transcription	Fetal Intestine Large	intestine
42	chr22:30133000-30140000	Strong transcription	Fetal Brain Female	brain
43	chr22:30133200-30136800	Strong transcription	Gastric	stomach
44	chr22:30133200-30137600	Strong transcription	Thymus	Thymus
45	chr22:30133200-30139000	Strong transcription	Lung	lung
46	chr22:30133200-30139200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr22:30133200-30144600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr22:30133400-30137400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr22:30133400-30137400	Strong transcription	Fetal Thymus	thymus
50	chr22:30133400-30137600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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