Variant report

Variant	rs72962654
Chromosome Location	chr3:120469281-120469282
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:120459863..120463133-chr3:120465920..120470912,5	K562	blood:
2	chr3:120469262..120472636-chr3:120473122..120476515,3	MCF-7	breast:
3	chr3:120459962..120462838-chr3:120467772..120469479,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000153767	Chromatin interaction
ENSG00000144840	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs57378115	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72962660	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72962662	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007557	chr3:119892894-120764353	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv536706	chr3:119892894-120764353	Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv829699	chr3:120308332-120484695	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
4	nsv869548	chr3:120320731-121076337	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
5	nsv916869	chr3:120360281-120973169	Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
6	nsv877378	chr3:120381530-120606438	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
7	nsv1005396	chr3:120460741-120580319	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
8	esv1797756	chr3:120464660-120473719	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv829700	chr3:120469191-120675763	Strong transcription Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:120462400-120471400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr3:120462600-120495200	Weak transcription	Aorta	Aorta
3	chr3:120462800-120469400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr3:120462800-120469400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:120462800-120469400	Weak transcription	Placenta	Placenta
6	chr3:120462800-120469400	Weak transcription	Lung	lung
7	chr3:120462800-120469400	Weak transcription	Stomach Smooth Muscle	stomach
8	chr3:120462800-120469400	Weak transcription	HSMMtube	muscle
9	chr3:120462800-120472200	Weak transcription	Brain Cingulate Gyrus	brain
10	chr3:120462800-120473000	Weak transcription	Brain Anterior Caudate	brain
11	chr3:120462800-120483000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr3:120462800-120485600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr3:120462800-120499800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr3:120462800-120500000	Weak transcription	Gastric	stomach
15	chr3:120462800-120503000	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr3:120463000-120469400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr3:120463000-120469400	Weak transcription	Primary T cells from cord blood	blood
18	chr3:120463000-120469400	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr3:120463000-120469400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr3:120463000-120469400	Weak transcription	Duodenum Mucosa	Duodenum
21	chr3:120463000-120469400	Weak transcription	Esophagus	oesophagus
22	chr3:120463000-120469400	Weak transcription	Fetal Stomach	stomach
23	chr3:120463000-120469400	Weak transcription	Fetal Thymus	thymus
24	chr3:120463000-120469400	Weak transcription	Left Ventricle	heart
25	chr3:120463000-120469400	Weak transcription	Ovary	ovary
26	chr3:120463000-120469400	Weak transcription	Psoas Muscle	Psoas
27	chr3:120463000-120469400	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr3:120463000-120469400	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr3:120463000-120469400	Weak transcription	HSMM	muscle
30	chr3:120463000-120469400	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr3:120463000-120470000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr3:120463000-120472000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr3:120463000-120472000	Weak transcription	Stomach Mucosa	stomach
34	chr3:120463000-120472600	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr3:120463000-120473200	Weak transcription	NHLF	lung
36	chr3:120463000-120477800	Weak transcription	Spleen	Spleen
37	chr3:120463000-120482400	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr3:120463000-120484800	Weak transcription	K562	blood
39	chr3:120463000-120485600	Weak transcription	Pancreas	Pancrea
40	chr3:120463000-120485600	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr3:120463000-120485600	Weak transcription	HMEC	breast
42	chr3:120463000-120493600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr3:120463000-120496000	Weak transcription	Fetal Lung	lung
44	chr3:120463000-120499800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr3:120463000-120502000	Weak transcription	Colonic Mucosa	Colon
46	chr3:120463000-120504200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr3:120463000-120504800	Weak transcription	Fetal Brain Male	brain
48	chr3:120463200-120469400	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr3:120463200-120469400	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr3:120463200-120469400	Weak transcription	Primary T helper cells PMA-I stimulated	--

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