Variant report

Variant	rs73111210
Chromosome Location	chr12:47970732-47970733
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:47969970..47972142-chr12:47972144..47974115,2	K562	blood:
2	chr12:47959788..47962194-chr12:47969072..47971219,2	K562	blood:
3	chr12:47954626..47957338-chr12:47968383..47970833,2	K562	blood:
4	chr12:47969081..47971247-chr12:47974364..47977314,2	MCF-7	breast:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs12422974	0.88[AMR][1000 genomes]
rs12423789	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12426347	0.88[AMR][1000 genomes]
rs12426387	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12426849	0.88[AMR][1000 genomes]
rs2020962	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35044089	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73102120	0.88[AMR][1000 genomes]
rs73102125	0.88[AMR][1000 genomes]
rs73102127	0.88[AMR][1000 genomes]
rs73102140	0.88[AMR][1000 genomes]
rs73102148	0.88[AMR][1000 genomes]
rs73102151	0.88[AMR][1000 genomes]
rs73111212	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73111216	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73111217	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73111220	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73111226	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73111229	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73111231	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73111258	1.00[AMR][1000 genomes]
rs73113117	1.00[AMR][1000 genomes]
rs73113139	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73113143	1.00[AMR][1000 genomes]
rs73113159	1.00[AMR][1000 genomes]
rs73113161	1.00[AMR][1000 genomes]
rs7954764	0.88[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv558785	chr12:47740440-48044011	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	nsv832400	chr12:47840248-48024605	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv430507	chr12:47883933-48079507	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1051131	chr12:47883981-48016556	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv899056	chr12:47940764-48012390	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	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
7	nsv558786	chr12:47942029-48044011	Strong transcription Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv558787	chr12:47945797-47981313	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv558788	chr12:47945797-48012390	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	esv2761737	chr12:47946795-48045722	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv1053061	chr12:47946795-48045722	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv899057	chr12:47947551-48012390	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv1050043	chr12:47949004-48087218	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	nsv527728	chr12:47954597-48044506	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:47969200-47971600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr12:47969200-47971600	Enhancers	Fetal Brain Male	brain
3	chr12:47969200-47972600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr12:47969400-47971400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr12:47969400-47974400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr12:47969800-47970800	Flanking Active TSS	Brain Germinal Matrix	brain
7	chr12:47969800-47970800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
8	chr12:47969800-47970800	Enhancers	Fetal Stomach	stomach
9	chr12:47969800-47971200	Enhancers	Fetal Lung	lung
10	chr12:47969800-47971600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:47970000-47970800	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr12:47970000-47971200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr12:47970000-47971600	Enhancers	Rectal Smooth Muscle	rectum
14	chr12:47970200-47970800	Active TSS	Brain Anterior Caudate	brain
15	chr12:47970200-47971400	Enhancers	Colon Smooth Muscle	Colon
16	chr12:47970400-47970800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr12:47970400-47970800	Enhancers	Brain Angular Gyrus	brain
18	chr12:47970400-47971200	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr12:47970400-47971400	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr12:47970400-47973400	Weak transcription	Fetal Muscle Trunk	muscle
21	chr12:47970600-47970800	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr12:47970600-47971600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr12:47970600-47971800	Weak transcription	Fetal Muscle Leg	muscle
24	chr12:47970600-47972000	Enhancers	Fetal Brain Female	brain
25	chr12:47970600-47974000	Weak transcription	Ovary	ovary

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