Variant report

Variant	rs61327127
Chromosome Location	chr12:48124638-48124639
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:48123429..48125813-chr12:48228513..48231351,2	MCF-7	breast:
2	chr12:48123237..48125446-chr12:48212337..48215614,3	MCF-7	breast:
3	chr12:48121475..48125710-chr12:48127578..48130124,5	MCF-7	breast:
4	chr12:48124296..48127190-chr12:48166396..48170138,3	MCF-7	breast:
5	chr12:48122622..48126569-chr12:48133427..48136331,4	K562	blood:
6	chr12:48123494..48126163-chr12:48177951..48180667,2	MCF-7	breast:
7	chr12:48115954..48117583-chr12:48123112..48125553,2	K562	blood:

Variant related genes	Relation type
ENSG00000061273	Chromatin interaction
ENSG00000268069	Chromatin interaction
ENSG00000211584	Chromatin interaction
ENSG00000079337	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1859256	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57162394	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57691959	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58232701	0.96[AFR][1000 genomes]
rs58237186	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58280987	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58348653	1.00[AMR][1000 genomes]
rs58350284	1.00[AMR][1000 genomes]
rs58636268	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59421933	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60045275	1.00[AMR][1000 genomes]
rs60186089	0.83[AFR][1000 genomes]
rs60608560	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61033936	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61288073	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61446607	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61734364	1.00[AMR][1000 genomes]
rs61739888	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7300107	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7308032	0.91[AFR][1000 genomes]
rs7314320	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73300649	1.00[AMR][1000 genomes]
rs73300689	1.00[AMR][1000 genomes]
rs73300701	1.00[AMR][1000 genomes]
rs73302603	1.00[AMR][1000 genomes]
rs73302628	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73302629	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73302650	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73302653	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73302662	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73302664	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73302673	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73302677	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73302679	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73302681	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73302682	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73302698	0.89[AFR][1000 genomes]
rs757283	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7965816	1.00[AMR][1000 genomes]
rs877196	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs877197	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs877198	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs879177	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs879178	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs879179	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9738787	1.00[AMR][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	esv2751101	chr12:47940858-48126885	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats 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	30 gene(s)	inside rSNPs	diseases
2	esv1813565	chr12:48097697-48177858	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer 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	39 gene(s)	inside rSNPs	diseases
3	nsv470289	chr12:48110551-48180508	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv1051941	chr12:48114026-48233128	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	75 gene(s)	inside rSNPs	diseases
5	nsv541487	chr12:48114026-48233128	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	75 gene(s)	inside rSNPs	diseases
6	nsv1036804	chr12:48114026-48287048	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
7	nsv524967	chr12:48119562-48215180	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
8	nsv527470	chr12:48119955-48190166	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48102800-48125000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr12:48112000-48126800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr12:48112200-48125400	Weak transcription	Fetal Thymus	thymus
4	chr12:48112200-48127000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr12:48112600-48128600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr12:48114000-48134400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr12:48114200-48132600	Weak transcription	Primary B cells from cord blood	blood
8	chr12:48114600-48128800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr12:48115200-48126200	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr12:48115600-48133600	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr12:48115600-48134200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr12:48115600-48135000	Weak transcription	Primary T cells from cord blood	blood
13	chr12:48116200-48124800	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr12:48116200-48124800	Enhancers	Placenta	Placenta
15	chr12:48116200-48134000	Weak transcription	Primary hematopoietic stem cells	blood
16	chr12:48116800-48130200	Weak transcription	Aorta	Aorta
17	chr12:48117000-48129000	Weak transcription	Psoas Muscle	Psoas
18	chr12:48118200-48128800	Weak transcription	Fetal Intestine Small	intestine
19	chr12:48119000-48126000	Enhancers	NHDF-Ad	bronchial
20	chr12:48119200-48125000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr12:48119600-48125000	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr12:48119800-48128600	Weak transcription	Colonic Mucosa	Colon
23	chr12:48120400-48128600	Weak transcription	NH-A	brain
24	chr12:48121400-48125800	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr12:48122400-48124800	Enhancers	Adipose Nuclei	Adipose
26	chr12:48122400-48124800	Enhancers	Brain Anterior Caudate	brain
27	chr12:48122400-48124800	Enhancers	NHLF	lung
28	chr12:48122400-48125000	Enhancers	Fetal Muscle Trunk	muscle
29	chr12:48122400-48125000	Enhancers	Fetal Muscle Leg	muscle
30	chr12:48122600-48124800	Enhancers	HSMM	muscle
31	chr12:48122600-48125000	Enhancers	Muscle Satellite Cultured Cells	--
32	chr12:48122600-48125000	Enhancers	Fetal Stomach	stomach
33	chr12:48122800-48124800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr12:48122800-48124800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr12:48122800-48124800	Enhancers	Ovary	ovary
36	chr12:48122800-48124800	Enhancers	Osteobl	bone
37	chr12:48122800-48126400	Enhancers	Fetal Heart	heart
38	chr12:48123000-48125000	Enhancers	Pancreas	Pancrea
39	chr12:48123000-48125800	Weak transcription	Brain Cingulate Gyrus	brain
40	chr12:48123000-48128400	Weak transcription	Spleen	Spleen
41	chr12:48123200-48124800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr12:48123400-48124800	Enhancers	Stomach Mucosa	stomach
43	chr12:48123600-48124800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr12:48123600-48125600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr12:48123600-48127000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr12:48123600-48128600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr12:48123600-48128600	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr12:48123800-48124800	Enhancers	Fetal Lung	lung
49	chr12:48123800-48124800	Enhancers	Right Ventricle	heart
50	chr12:48123800-48125600	Weak transcription	Brain Hippocampus Middle	brain

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