Variant report

Variant	rs10414945
Chromosome Location	chr19:35802214-35802215
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:35761264..35763399-chr19:35801388..35804082,2	K562	blood:
2	chr19:35738491..35740445-chr19:35800431..35803185,3	MCF-7	breast:
3	chr19:35757352..35763490-chr19:35798817..35804347,10	MCF-7	breast:
4	chr19:35606400..35608352-chr19:35800705..35803047,2	MCF-7	breast:
5	chr19:35755149..35764508-chr19:35799437..35813142,44	MCF-7	breast:
6	chr19:35801834..35808584-chr19:35810190..35813576,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000105699	Chromatin interaction
ENSG00000089356	Chromatin interaction
ENSG00000105698	Chromatin interaction
ENSG00000012124	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10414549	0.94[EUR][1000 genomes]
rs1858852	0.86[AFR][1000 genomes]
rs2269757	0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432045	chr19:35556260-36520760	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv1060100	chr19:35658505-36170042	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv543993	chr19:35658505-36170042	Enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer 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	107 gene(s)	inside rSNPs	diseases
4	nsv510765	chr19:35708226-35890668	Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
5	esv2758497	chr19:35711078-35887113	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
6	esv2758758	chr19:35711078-35887113	Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
7	nsv911618	chr19:35734107-35807845	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
8	nsv833810	chr19:35782588-35971959	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
9	nsv9711	chr19:35797190-35805196	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	n/a
10	esv1006379	chr19:35798572-35810821	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35774800-35809600	Weak transcription	Right Atrium	heart
2	chr19:35794400-35810000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr19:35797600-35804000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr19:35797800-35809600	Weak transcription	Brain Angular Gyrus	brain
5	chr19:35798000-35802600	Enhancers	Placenta	Placenta
6	chr19:35798200-35802800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr19:35798200-35811400	Weak transcription	Liver	Liver
8	chr19:35799200-35804000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr19:35799400-35804200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr19:35799600-35803400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr19:35800000-35803800	Strong transcription	Brain Inferior Temporal Lobe	brain
12	chr19:35800000-35804000	Weak transcription	Primary B cells from cord blood	blood
13	chr19:35800200-35803400	Enhancers	Placenta Amnion	Placenta Amnion
14	chr19:35800400-35802600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr19:35800600-35803400	Flanking Active TSS	Ovary	ovary
16	chr19:35800800-35805200	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr19:35800800-35806600	Enhancers	HepG2	liver
18	chr19:35801000-35803000	Enhancers	Fetal Thymus	thymus
19	chr19:35801000-35809400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr19:35801200-35803000	Weak transcription	Fetal Intestine Large	intestine
21	chr19:35801400-35803200	Enhancers	Primary B cells from peripheral blood	blood
22	chr19:35801400-35803200	Strong transcription	Brain Cingulate Gyrus	brain
23	chr19:35801400-35804400	Enhancers	Hela-S3	cervix
24	chr19:35801400-35804800	Strong transcription	Brain Hippocampus Middle	brain
25	chr19:35801600-35802400	Enhancers	Fetal Kidney	kidney
26	chr19:35801600-35804200	Weak transcription	Spleen	Spleen
27	chr19:35801600-35805200	Enhancers	K562	blood
28	chr19:35801800-35802800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr19:35801800-35802800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr19:35801800-35804200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr19:35802000-35802400	Weak transcription	Thymus	Thymus
32	chr19:35802000-35802400	Weak transcription	HMEC	breast
33	chr19:35802000-35802600	Weak transcription	Fetal Lung	lung
34	chr19:35802000-35802800	Weak transcription	Brain Substantia Nigra	brain
35	chr19:35802000-35804000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr19:35802200-35803200	Strong transcription	Brain Anterior Caudate	brain

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