Variant report

Variant	rs13057011
Chromosome Location	chr22:29177137-29177138
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr22:29172058..29177577-chr22:29178390..29181662,9	MCF-7	breast:
2	chr22:29175268..29177252-chr22:29194903..29197357,4	MCF-7	breast:
3	chr22:29165791..29171536-chr22:29171828..29178249,15	MCF-7	breast:
4	chr22:29175785..29179613-chr22:29195586..29198060,4	K562	blood:
5	chr22:29004756..29007074-chr22:29174850..29177158,2	K562	blood:
6	chr22:29167384..29172904-chr22:29173066..29177227,7	K562	blood:

Variant related genes	Relation type
ENSG00000100219	Chromatin interaction
ENSG00000226471	Chromatin interaction
ENSG00000159873	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs12165715	1.00[CHB][hapmap]
rs12165893	1.00[CHB][hapmap]
rs12166245	1.00[CHB][hapmap]
rs12166716	1.00[CHB][hapmap]
rs12168765	1.00[CHB][hapmap]
rs12169262	1.00[CHB][hapmap]
rs12169460	1.00[CHB][hapmap]
rs17880867	1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs17885263	1.00[TSI][hapmap]
rs28909980	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap]
rs7289534	1.00[CHB][hapmap]
rs7293232	1.00[CHB][hapmap]
rs9613680	1.00[CHD][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs9620808	1.00[CHB][hapmap]
rs9620810	1.00[CHB][hapmap]
rs9620811	1.00[CHB][hapmap]
rs9620826	1.00[CHB][hapmap]
rs9620828	1.00[CHB][hapmap]
rs9625512	1.00[CHB][hapmap]
rs9625513	1.00[CHB][hapmap]
rs9625514	1.00[CHB][hapmap]
rs9625520	1.00[CHB][hapmap]
rs9625521	1.00[CHB][hapmap]
rs9625523	1.00[CHB][hapmap]
rs9625524	1.00[CHB][hapmap]
rs9625554	1.00[CHB][hapmap]

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	nsv916473	chr22:28837041-29215603	Weak transcription Bivalent Enhancer Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
2	nsv9895	chr22:29029961-29184277	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv1064079	chr22:29065528-29456059	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
4	nsv834169	chr22:29095446-29303929	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
5	esv3517058	chr22:29176967-29179307	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
6	esv3517059	chr22:29176967-29179307	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	esv2430624	chr22:29177114-29178745	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
8	esv2307652	chr22:29177124-29177718	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29169800-29179600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr22:29169800-29180000	Weak transcription	Colonic Mucosa	Colon
3	chr22:29169800-29180200	Weak transcription	Stomach Mucosa	stomach
4	chr22:29169800-29190400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr22:29170000-29177600	Weak transcription	Aorta	Aorta
6	chr22:29170000-29179200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr22:29170000-29179600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr22:29170000-29182200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr22:29170000-29190200	Weak transcription	Fetal Heart	heart
10	chr22:29170000-29194200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr22:29170200-29177800	Weak transcription	HMEC	breast
12	chr22:29170200-29178000	Weak transcription	Brain Anterior Caudate	brain
13	chr22:29170200-29178800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr22:29170200-29182400	Strong transcription	Fetal Stomach	stomach
15	chr22:29170400-29177800	Strong transcription	Fetal Intestine Large	intestine
16	chr22:29170400-29183800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr22:29170400-29184000	Strong transcription	Fetal Muscle Leg	muscle
18	chr22:29170400-29185600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr22:29170600-29184600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr22:29170600-29184800	Strong transcription	Fetal Muscle Trunk	muscle
21	chr22:29170600-29185400	Strong transcription	HUES64 Cell Line	embryonic stem cell
22	chr22:29170600-29186000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr22:29170600-29186400	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr22:29170800-29179800	Weak transcription	Fetal Brain Male	brain
25	chr22:29170800-29186400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr22:29171000-29178000	Weak transcription	Brain Angular Gyrus	brain
27	chr22:29171000-29179600	Weak transcription	Small Intestine	intestine
28	chr22:29171000-29185600	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr22:29171200-29178600	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr22:29171200-29179000	Weak transcription	Brain Substantia Nigra	brain
31	chr22:29171200-29179200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr22:29171200-29186800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr22:29171200-29188600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr22:29171400-29179600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr22:29171400-29186000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr22:29171600-29178000	Weak transcription	Fetal Kidney	kidney
37	chr22:29171800-29178000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr22:29171800-29186200	Strong transcription	Fetal Thymus	thymus
39	chr22:29172000-29179400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr22:29172200-29177800	Weak transcription	Brain Germinal Matrix	brain
41	chr22:29172200-29179600	Weak transcription	NHLF	lung
42	chr22:29172400-29178000	Weak transcription	Right Ventricle	heart
43	chr22:29172400-29178000	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr22:29172400-29179200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr22:29172400-29179400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr22:29172400-29186200	Strong transcription	Placenta	Placenta
47	chr22:29172600-29184200	Strong transcription	Primary B cells from peripheral blood	blood
48	chr22:29173000-29178600	Weak transcription	A549	lung
49	chr22:29173200-29185600	Strong transcription	Left Ventricle	heart
50	chr22:29173600-29179200	Strong transcription	Sigmoid Colon	Sigmoid Colon

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