Variant report

Variant	rs4774756
Chromosome Location	chr15:55547057-55547058
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:55529333..55531848-chr15:55546495..55549479,2	K562	blood:
2	chr15:55541209..55543610-chr15:55545999..55547542,2	K562	blood:
3	chr15:55546620..55548726-chr15:55579934..55582507,2	K562	blood:
4	chr15:55533451..55535034-chr15:55546175..55548758,2	K562	blood:
5	chr15:55545838..55548100-chr15:55559043..55560883,2	K562	blood:
6	chr15:55532304..55535313-chr15:55545055..55548758,3	K562	blood:
7	chr15:55545068..55547245-chr15:55548982..55551880,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000069974	Chromatin interaction

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

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

rs_ID	r²[population]
rs12910930	0.91[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs2444039	1.00[CEU][hapmap];0.82[CHB][hapmap];0.90[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2444043	0.90[JPT][hapmap]
rs3784547	0.85[AMR][1000 genomes]
rs3985771	0.90[JPT][hapmap]
rs498712	0.83[ASN][1000 genomes]
rs517707	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs525152	0.83[ASN][1000 genomes]
rs540476	0.90[JPT][hapmap]
rs62018087	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9920114	1.00[CEU][hapmap];0.90[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9920645	0.90[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	nsv1043176	chr15:55010228-55563000	Genic enhancers Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1042741	chr15:55068022-55622497	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv1039471	chr15:55137606-55552555	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv917323	chr15:55290499-56041334	Genic enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
5	nsv1043789	chr15:55400872-56092454	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
6	nsv1049977	chr15:55502508-55555694	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1036924	chr15:55527874-55616480	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv1051046	chr15:55529291-55821973	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS 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 miRNA target site	36 gene(s)	inside rSNPs	diseases
9	nsv569522	chr15:55532211-55611126	Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
10	nsv904241	chr15:55534342-55611126	Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55490000-55562800	Weak transcription	Ovary	ovary
2	chr15:55514800-55560400	Weak transcription	Spleen	Spleen
3	chr15:55516000-55559600	Weak transcription	Fetal Stomach	stomach
4	chr15:55520800-55574800	Weak transcription	Stomach Smooth Muscle	stomach
5	chr15:55538600-55549000	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr15:55540600-55561200	Weak transcription	Esophagus	oesophagus
7	chr15:55541200-55549000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr15:55541400-55547200	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr15:55541800-55547800	Weak transcription	Left Ventricle	heart
10	chr15:55542400-55547200	Weak transcription	Aorta	Aorta
11	chr15:55542400-55581000	Weak transcription	Fetal Intestine Small	intestine
12	chr15:55543400-55550600	Weak transcription	Fetal Kidney	kidney
13	chr15:55543600-55547400	Weak transcription	Duodenum Mucosa	Duodenum
14	chr15:55543600-55547400	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr15:55543600-55548400	Weak transcription	NHEK	skin
16	chr15:55543600-55559200	Weak transcription	Hela-S3	cervix
17	chr15:55543800-55547200	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr15:55543800-55547400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr15:55543800-55547600	Weak transcription	Fetal Thymus	thymus
20	chr15:55543800-55547600	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr15:55543800-55559400	Weak transcription	Thymus	Thymus
22	chr15:55544400-55548400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr15:55544400-55558800	Weak transcription	Right Ventricle	heart
24	chr15:55544600-55547200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr15:55544800-55557800	Weak transcription	Pancreas	Pancrea
26	chr15:55545000-55547200	Weak transcription	Liver	Liver
27	chr15:55545200-55549000	Enhancers	Stomach Mucosa	stomach
28	chr15:55545200-55561000	Weak transcription	Lung	lung
29	chr15:55545400-55547200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr15:55545400-55547200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr15:55545400-55547400	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr15:55545600-55547200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr15:55545600-55547200	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr15:55545800-55547200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr15:55545800-55547200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr15:55545800-55547600	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr15:55545800-55548200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr15:55546000-55547200	Weak transcription	Primary B cells from cord blood	blood
39	chr15:55546000-55547200	Weak transcription	Small Intestine	intestine
40	chr15:55546000-55547400	Weak transcription	HepG2	liver
41	chr15:55546200-55547200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr15:55546200-55547200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr15:55546200-55547200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr15:55546200-55547200	Weak transcription	K562	blood
45	chr15:55546200-55547200	Weak transcription	NHLF	lung
46	chr15:55546200-55547600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr15:55546200-55547600	Weak transcription	HUVEC	blood vessel
48	chr15:55546200-55547800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr15:55546200-55559200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr15:55546200-55559800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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