Variant report

Variant	rs60408515
Chromosome Location	chr1:228125326-228125327
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:227950090..227952610-chr1:228122891..228125327,3	MCF-7	breast:
2	chr1:228120999..228125449-chr1:228127251..228129340,4	MCF-7	breast:
3	chr1:228124987..228127284-chr1:228134040..228136968,3	MCF-7	breast:
4	chr1:228125046..228126642-chr1:228127676..228130531,2	K562	blood:
5	chr1:228124876..228126546-chr1:228127658..228129176,2	K562	blood:

Variant related genes	Relation type
ENSG00000143816	Chromatin interaction
ENSG00000264483	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1155358	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13373831	0.86[ASN][1000 genomes]
rs56772497	0.91[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs58978756	0.82[ASN][1000 genomes]
rs6426490	0.83[ASN][1000 genomes]
rs6675355	0.82[ASN][1000 genomes]
rs6701785	0.83[ASN][1000 genomes]
rs7515849	0.87[ASN][1000 genomes]
rs7517798	0.87[ASN][1000 genomes]
rs7529664	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7541491	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs881398	0.81[ASN][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	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
2	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
3	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
4	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
5	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
6	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
7	nsv516409	chr1:228035131-228296745	Enhancers Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
8	nsv523935	chr1:228038124-228681749	Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	137 gene(s)	inside rSNPs	diseases
9	nsv873251	chr1:228051234-228160911	Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
10	esv1837581	chr1:228122234-228127227	Strong transcription ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228107800-228134400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:228109600-228132000	Weak transcription	Gastric	stomach
3	chr1:228109800-228134000	Weak transcription	Right Atrium	heart
4	chr1:228111000-228129800	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr1:228118000-228125400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:228118000-228126000	Weak transcription	Esophagus	oesophagus
7	chr1:228118400-228133000	Weak transcription	Ovary	ovary
8	chr1:228119000-228128000	Weak transcription	Pancreas	Pancrea
9	chr1:228121000-228132600	Weak transcription	Fetal Intestine Small	intestine
10	chr1:228121800-228128200	Weak transcription	Psoas Muscle	Psoas
11	chr1:228123200-228125800	Weak transcription	Colon Smooth Muscle	Colon
12	chr1:228123400-228125400	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr1:228123400-228125400	Strong transcription	HSMMtube	muscle
14	chr1:228123400-228126200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr1:228123600-228125600	Strong transcription	Fetal Muscle Leg	muscle
16	chr1:228123800-228128600	Weak transcription	HSMM	muscle
17	chr1:228123800-228132000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr1:228123800-228132600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr1:228124200-228125600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr1:228124200-228126000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr1:228124200-228126200	Strong transcription	Fetal Stomach	stomach
22	chr1:228124400-228125600	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr1:228124400-228125800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:228124400-228125800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:228124400-228126000	Enhancers	Placenta Amnion	Placenta Amnion
26	chr1:228124600-228125400	Enhancers	Primary hematopoietic stem cells	blood
27	chr1:228124600-228125400	ZNF genes & repeats	HMEC	breast
28	chr1:228124600-228126000	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr1:228124800-228125400	Strong transcription	Fetal Muscle Trunk	muscle
30	chr1:228124800-228128200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr1:228125000-228125400	Active TSS	Spleen	Spleen
32	chr1:228125200-228125400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr1:228125200-228125400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr1:228125200-228125400	Weak transcription	Stomach Smooth Muscle	stomach
35	chr1:228125200-228125800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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