Variant report

Variant	rs7157676
Chromosome Location	chr14:67833686-67833687
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:67831647..67837851-chr14:67838094..67843638,9	K562	blood:
2	chr14:67828950..67831187-chr14:67833390..67835358,2	MCF-7	breast:
3	chr14:67824949..67830846-chr14:67831732..67836523,8	K562	blood:
4	chr14:67833401..67836470-chr14:67837034..67842117,5	K562	blood:

Variant related genes	Relation type
ENSG00000100554	Chromatin interaction
ENSG00000134001	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10083528	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10129218	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10135565	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10136835	0.84[EUR][1000 genomes]
rs10140203	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10141049	0.84[EUR][1000 genomes]
rs10144002	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10145458	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs10148114	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10150612	0.84[EUR][1000 genomes]
rs13379087	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13379190	1.00[CEU][hapmap];1.00[GIH][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes]
rs13379449	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28410937	0.84[EUR][1000 genomes]
rs28477898	1.00[ASN][1000 genomes]
rs28503899	0.84[EUR][1000 genomes]
rs35236021	0.84[EUR][1000 genomes]
rs57402080	0.85[EUR][1000 genomes]
rs59231326	0.85[EUR][1000 genomes]
rs59984712	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6573767	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7149826	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7154820	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7342569	1.00[CEU][hapmap];1.00[GIH][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap]
rs8008820	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8012994	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[YRI][hapmap];0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8013980	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes]
rs8014465	0.84[EUR][1000 genomes]
rs8015912	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs8016480	0.84[EUR][1000 genomes]
rs8020334	1.00[CEU][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8021740	0.90[ASW][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap]
rs8022938	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[YRI][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751285	chr14:67364747-67886781	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv1045518	chr14:67529049-67959582	Strong transcription Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv456331	chr14:67732861-68103780	Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv564961	chr14:67732861-68103780	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers 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	41 gene(s)	inside rSNPs	diseases
5	nsv470651	chr14:67732861-68113293	Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
6	nsv1054389	chr14:67804987-67922598	Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
7	nsv542121	chr14:67804987-67922598	Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67827800-67834000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:67827800-67834000	Weak transcription	Gastric	stomach
3	chr14:67827800-67834800	Weak transcription	Esophagus	oesophagus
4	chr14:67828200-67841600	Weak transcription	Aorta	Aorta
5	chr14:67828400-67837800	Weak transcription	Right Ventricle	heart
6	chr14:67828400-67854000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr14:67828600-67838000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr14:67828600-67854600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr14:67828800-67854000	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr14:67829000-67855200	Strong transcription	Fetal Thymus	thymus
11	chr14:67829200-67836400	Strong transcription	NH-A	brain
12	chr14:67829200-67852000	Strong transcription	Placenta	Placenta
13	chr14:67829200-67853200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr14:67829200-67853600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
15	chr14:67829400-67838200	Weak transcription	Stomach Mucosa	stomach
16	chr14:67829400-67841200	Genic enhancers	Primary T helper cells PMA-I stimulated	--
17	chr14:67829400-67853600	Strong transcription	Primary B cells from peripheral blood	blood
18	chr14:67829400-67854000	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr14:67829400-67854200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr14:67829400-67854200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
21	chr14:67829600-67854800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr14:67829800-67834200	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr14:67829800-67837200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr14:67829800-67838600	Strong transcription	Brain Hippocampus Middle	brain
25	chr14:67829800-67839400	Strong transcription	Rectal Mucosa Donor 31	rectum
26	chr14:67829800-67843200	Weak transcription	Fetal Heart	heart
27	chr14:67829800-67854000	Strong transcription	HUES6 Cell Line	embryonic stem cell
28	chr14:67829800-67854400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr14:67830000-67834000	Genic enhancers	Dnd41	blood
30	chr14:67830000-67837000	Strong transcription	HMEC	breast
31	chr14:67830000-67837000	Strong transcription	NHDF-Ad	bronchial
32	chr14:67830000-67837200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr14:67830000-67854000	Strong transcription	HSMM	muscle
34	chr14:67830200-67851800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr14:67830400-67838200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr14:67830400-67854000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr14:67830400-67855000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr14:67830400-67855000	Strong transcription	Liver	Liver
39	chr14:67830600-67836400	Strong transcription	K562	blood
40	chr14:67830600-67838400	Strong transcription	Primary hematopoietic stem cells	blood
41	chr14:67830800-67836200	Strong transcription	HUVEC	blood vessel
42	chr14:67830800-67837200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr14:67830800-67853000	Strong transcription	Cortex derived primary cultured neurospheres	brain
44	chr14:67831000-67837600	Strong transcription	A549	lung
45	chr14:67831000-67854000	Strong transcription	Primary monocytes fromperipheralblood	blood
46	chr14:67831000-67855200	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr14:67831200-67834800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr14:67831200-67836400	Strong transcription	Hela-S3	cervix
49	chr14:67831200-67854600	Strong transcription	Primary T cells from cord blood	blood
50	chr14:67831200-67864600	Strong transcription	Duodenum Mucosa	Duodenum

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