Variant report

Variant	rs754224
Chromosome Location	chr1:227963491-227963492
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:227960240..227967392-chr1:227972741..227977657,8	K562	blood:
2	chr1:227962379..227965351-chr1:228135797..228137632,2	MCF-7	breast:
3	chr1:227962656..227964965-chr1:227972636..227975785,3	MCF-7	breast:
4	chr1:227962393..227964421-chr1:227964813..227967727,3	MCF-7	breast:
5	chr1:227963179..227967609-chr1:227968212..227971433,3	K562	blood:

Extended variants
information (count: 16 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs12123869	0.85[EUR][1000 genomes]
rs3087908	0.88[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];0.96[TSI][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4653867	0.88[MEX][hapmap];0.81[TSI][hapmap]
rs751748	0.81[CEU][hapmap];0.88[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];0.82[MEX][hapmap];0.96[TSI][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534002	chr1:227315186-228047108	Bivalent/Poised TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
2	nsv1007479	chr1:227695868-227984466	Genic enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv1010605	chr1:227770415-228332690	Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
4	esv32853	chr1:227880116-228806209	Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases
5	nsv427952	chr1:227881664-228308629	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
6	nsv826908	chr1:227895386-228691100	Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
7	nsv515496	chr1:227912474-227967938	Active TSS Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
8	nsv873249	chr1:227920061-228121548	Weak transcription Bivalent Enhancer Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
9	nsv468238	chr1:227935762-228045748	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv549272	chr1:227935762-228045748	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS 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	9 gene(s)	inside rSNPs	diseases
11	nsv1005852	chr1:227957099-228148363	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
12	nsv535319	chr1:227957099-228148363	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs754224	ZNF678	Cis_1M	lymphoblastoid	RTeQTL
rs754224	ZNF678	cis	normal skin	skin_eQTL
rs754224	ZNF678	cis	lesional skin	skin_eQTL
rs754224	ZNF678	cis	uninvolved skin	skin_eQTL

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227950800-227974200	Weak transcription	Small Intestine	intestine
2	chr1:227951200-227974400	Weak transcription	Right Atrium	heart
3	chr1:227951600-227963600	Weak transcription	HUVEC	blood vessel
4	chr1:227951800-227970600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:227954400-227963800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:227954400-227974600	Weak transcription	HMEC	breast
7	chr1:227954800-227964400	Strong transcription	Primary B cells from peripheral blood	blood
8	chr1:227955200-227964800	Strong transcription	Liver	Liver
9	chr1:227955600-227965000	Strong transcription	Placenta	Placenta
10	chr1:227955600-227973200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr1:227955600-227974000	Weak transcription	Fetal Brain Male	brain
12	chr1:227955800-227972400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr1:227955800-227974800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:227955800-227975200	Weak transcription	Hela-S3	cervix
15	chr1:227956000-227964200	Weak transcription	Fetal Kidney	kidney
16	chr1:227956000-227964600	Strong transcription	Sigmoid Colon	Sigmoid Colon
17	chr1:227956000-227974600	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr1:227956200-227968000	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr1:227956600-227973000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr1:227956800-227963600	Weak transcription	GM12878-XiMat	blood
21	chr1:227957000-227966200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:227957000-227968200	Weak transcription	Aorta	Aorta
23	chr1:227957000-227970000	Weak transcription	K562	blood
24	chr1:227957000-227970400	Strong transcription	Fetal Intestine Small	intestine
25	chr1:227957200-227963600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:227957600-227972800	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr1:227957800-227963600	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr1:227957800-227967200	Weak transcription	NHEK	skin
29	chr1:227957800-227974600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr1:227958000-227975200	Weak transcription	A549	lung
31	chr1:227958400-227963600	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr1:227958400-227963600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr1:227958600-227963600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr1:227958600-227967200	Weak transcription	Brain Substantia Nigra	brain
35	chr1:227958800-227963600	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr1:227959000-227963600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr1:227959200-227964200	Weak transcription	Brain Angular Gyrus	brain
38	chr1:227960400-227963600	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr1:227960600-227963600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr1:227961200-227964000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr1:227961200-227964600	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr1:227961200-227969200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr1:227961400-227964400	Strong transcription	Lung	lung
44	chr1:227961400-227967400	Strong transcription	Spleen	Spleen
45	chr1:227961400-227967800	Enhancers	HSMMtube	muscle
46	chr1:227961600-227964400	Strong transcription	Gastric	stomach
47	chr1:227961600-227964600	Strong transcription	Dnd41	blood
48	chr1:227961800-227964400	Enhancers	Fetal Heart	heart
49	chr1:227961800-227964600	Genic enhancers	Fetal Stomach	stomach
50	chr1:227961800-227965200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood

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