Variant report

Variant	rs1561867
Chromosome Location	chr15:99974840-99974841
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZBTB7A	chr15:99974716-99976264	ECC-1	luminal epithelium:	n/a	chr15:99975497-99975508

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:99973224..99976448-chr15:99991050..99995157,5	MCF-7	breast:
2	chr15:99962979..99964880-chr15:99972892..99975204,2	MCF-7	breast:
3	chr15:99971316..99975999-chr15:100104042..100107403,7	MCF-7	breast:
4	chr15:99972525..99976931-chr15:99986719..99991606,5	MCF-7	breast:
5	chr15:99974033..99977897-chr15:99978912..99982934,5	K562	blood:
6	chr15:99972394..99975109-chr15:99977541..99980166,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000259341	TF binding region
ENSG00000068305	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs28401581	1.00[AMR][1000 genomes]
rs28538075	1.00[AMR][1000 genomes]
rs28625704	1.00[AMR][1000 genomes]
rs28627884	1.00[AMR][1000 genomes]
rs28703866	1.00[AMR][1000 genomes]
rs28738845	1.00[AMR][1000 genomes]
rs4965232	1.00[AMR][1000 genomes]
rs56666565	1.00[AMR][1000 genomes]
rs58562373	1.00[AMR][1000 genomes]
rs58649201	1.00[AMR][1000 genomes]
rs59299420	1.00[AMR][1000 genomes]
rs60632743	1.00[AMR][1000 genomes]
rs73473392	1.00[AMR][1000 genomes]
rs73476566	1.00[AMR][1000 genomes]
rs73476567	1.00[AMR][1000 genomes]
rs73476570	1.00[AMR][1000 genomes]
rs73476572	1.00[AMR][1000 genomes]
rs73476579	1.00[AMR][1000 genomes]
rs73476580	1.00[AMR][1000 genomes]
rs73476583	1.00[AMR][1000 genomes]
rs73476584	1.00[AMR][1000 genomes]
rs73476586	1.00[AMR][1000 genomes]
rs73476597	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055008	chr15:99477144-100019861	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
2	nsv904543	chr15:99513231-99991506	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv533926	chr15:99519820-99997114	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	nsv915926	chr15:99519820-100138705	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
5	nsv817289	chr15:99621061-100138705	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
6	nsv431411	chr15:99621061-100143999	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
7	nsv904546	chr15:99696046-100166300	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
8	nsv1036346	chr15:99752391-100365458	Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
9	nsv542520	chr15:99752391-100365458	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
10	nsv1051560	chr15:99837102-100124483	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
11	nsv817201	chr15:99839238-100537341	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
12	nsv904547	chr15:99940221-99979159	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv904548	chr15:99940221-99979418	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv904549	chr15:99940221-99991506	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
15	nsv519800	chr15:99950772-99987109	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
16	nsv904550	chr15:99954278-99978524	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
17	nsv904551	chr15:99954278-99979418	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
18	nsv904552	chr15:99954278-99982447	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
19	nsv904553	chr15:99954278-99983175	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
20	nsv904554	chr15:99956954-99979418	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
21	nsv904555	chr15:99956954-99981269	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
22	nsv904556	chr15:99956954-99987109	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
23	nsv904557	chr15:99956954-99991506	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
24	nsv519319	chr15:99972661-99991506	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
25	nsv570728	chr15:99973369-99986764	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:99966800-99975400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr15:99970000-99976800	Enhancers	Primary B cells from peripheral blood	blood
3	chr15:99971200-99978000	Enhancers	Spleen	Spleen
4	chr15:99971400-99978800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr15:99971400-99979200	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr15:99971600-99978800	Enhancers	Primary T cells from cord blood	blood
7	chr15:99971800-99976400	Enhancers	Primary B cells from cord blood	blood
8	chr15:99972000-99975200	Enhancers	Esophagus	oesophagus
9	chr15:99972000-99976000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr15:99972000-99976600	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr15:99972200-99976200	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr15:99972200-99978600	Enhancers	Fetal Thymus	thymus
13	chr15:99972400-99975800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr15:99972400-99977400	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr15:99972600-99975200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr15:99972600-99975200	Enhancers	HMEC	breast
17	chr15:99972600-99975600	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr15:99972600-99976400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr15:99972600-99976600	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr15:99972600-99977400	Enhancers	Placenta Amnion	Placenta Amnion
21	chr15:99972600-99979000	Enhancers	Left Ventricle	heart
22	chr15:99972800-99975000	Enhancers	GM12878-XiMat	blood
23	chr15:99972800-99976400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr15:99972800-99977800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr15:99972800-99978800	Enhancers	Lung	lung
26	chr15:99972800-99979000	Enhancers	Adipose Nuclei	Adipose
27	chr15:99973000-99975200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr15:99973200-99975200	Enhancers	Duodenum Mucosa	Duodenum
29	chr15:99973200-99976800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
30	chr15:99973200-99977000	Enhancers	Stomach Mucosa	stomach
31	chr15:99973400-99975000	Enhancers	Hela-S3	cervix
32	chr15:99973400-99975200	Weak transcription	Rectal Smooth Muscle	rectum
33	chr15:99973400-99976200	Enhancers	Fetal Intestine Small	intestine
34	chr15:99973400-99978600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
35	chr15:99973600-99975000	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr15:99973600-99975200	Enhancers	Brain Anterior Caudate	brain
37	chr15:99973600-99975800	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr15:99973600-99976400	Enhancers	Fetal Lung	lung
39	chr15:99973800-99975000	Weak transcription	Primary hematopoietic stem cells	blood
40	chr15:99973800-99975400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr15:99973800-99975600	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr15:99973800-99975600	Weak transcription	Colon Smooth Muscle	Colon
43	chr15:99973800-99977000	Weak transcription	Ovary	ovary
44	chr15:99973800-99978000	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr15:99973800-99978400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr15:99974000-99975000	Weak transcription	Thymus	Thymus
47	chr15:99974000-99975600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr15:99974000-99976400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr15:99974000-99977600	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr15:99974000-99977800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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