Variant report

Variant	rs4077585
Chromosome Location	chr15:74666631-74666632
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr15:74665429..74667664-chr15:74747982..74750255,2	MCF-7	breast:
2	chr15:74665025..74668014-chr15:74668385..74670407,3	MCF-7	breast:
3	chr15:74664518..74667093-chr15:74731124..74732993,2	MCF-7	breast:
4	chr15:74665902..74667600-chr15:74730654..74731665,8	K562	blood:
5	chr15:74664221..74666874-chr15:74684631..74687435,2	K562	blood:
6	chr15:74665952..74666781-chr15:75062636..75063591,2	MCF-7	breast:
7	chr15:74665092..74667430-chr15:74726842..74729796,2	K562	blood:
8	chr15:74664672..74667592-chr15:74837544..74840546,3	MCF-7	breast:
9	chr15:74666571..74668341-chr15:75112633..75114980,2	MCF-7	breast:
10	chr15:74666062..74666780-chr15:74733316..74734121,2	K562	blood:
11	chr15:74665889..74666878-chr15:74913167..74914585,8	MCF-7	breast:
12	chr15:74665365..74667927-chr15:74780037..74785377,6	MCF-7	breast:
13	chr15:74665674..74667087-chr15:74730530..74731799,6	MCF-7	breast:
14	chr15:74665357..74666676-chr15:74923962..74924983,9	K562	blood:
15	chr15:74664841..74669022-chr15:74717731..74721779,3	K562	blood:
16	chr15:74664899..74666898-chr15:74740722..74743644,2	K562	blood:
17	chr15:74665425..74667643-chr15:74752949..74754890,2	K562	blood:
18	chr15:74665745..74666851-chr15:74913129..74914141,6	MCF-7	breast:
19	chr15:74665680..74666890-chr15:75060904..75061896,5	K562	blood:
20	chr15:74665568..74668523-chr15:74922376..74925547,4	MCF-7	breast:
21	chr15:74666064..74667583-chr15:74922840..74924657,2	MCF-7	breast:
22	chr15:74662886..74664620-chr15:74666174..74668404,2	MCF-7	breast:
23	chr15:74665982..74668403-chr15:74893258..74895614,2	MCF-7	breast:
24	chr15:74665122..74667877-chr15:74906569..74911881,5	MCF-7	breast:
25	chr15:74665832..74668344-chr15:74734420..74737401,2	K562	blood:
26	chr15:74665248..74670570-chr15:74911003..74915113,6	MCF-7	breast:
27	chr15:74666257..74668996-chr15:74908771..74912295,3	K562	blood:
28	chr15:74346274..74346810-chr15:74666060..74666858,2	MCF-7	breast:
29	chr15:74666408..74668530-chr15:74918193..74920965,2	MCF-7	breast:
30	chr15:74666244..74667848-chr15:74753089..74754898,2	MCF-7	breast:
31	chr15:74665453..74667821-chr15:74780445..74783665,3	MCF-7	breast:
32	chr15:74664932..74669170-chr15:74905600..74910371,8	K562	blood:
33	chr15:74665255..74670127-chr15:74905870..74910808,10	MCF-7	breast:
34	chr15:74665619..74667467-chr17:66287023..66289875,2	MCF-7	breast:
35	chr15:74666116..74667931-chr15:74831912..74834026,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000140506	Chromatin interaction
ENSG00000212279	Chromatin interaction
ENSG00000108932	Chromatin interaction
ENSG00000179361	Chromatin interaction
ENSG00000261775	Chromatin interaction
ENSG00000141337	Chromatin interaction
ENSG00000260103	Chromatin interaction
ENSG00000247240	Chromatin interaction
ENSG00000261606	Chromatin interaction
ENSG00000260919	Chromatin interaction
ENSG00000138629	Chromatin interaction
ENSG00000179335	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs12438594	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16968477	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs16968478	0.92[ASN][1000 genomes]
rs2073475	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28681535	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3825944	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3935523	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4077581	0.86[AFR][1000 genomes]
rs4077583	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4077584	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4555110	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4598865	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60636222	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7167038	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7180275	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7181947	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428641	chr15:74555113-74724630	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
2	nsv482615	chr15:74593625-74757962	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
3	nsv904351	chr15:74638965-74697084	Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	nsv904352	chr15:74638965-74715205	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74665600-74667800	Flanking Active TSS	Hela-S3	cervix
2	chr15:74665800-74667000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
3	chr15:74665800-74667200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
4	chr15:74665800-74667600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr15:74665800-74667600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr15:74665800-74667600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr15:74665800-74667800	Enhancers	Fetal Heart	heart
8	chr15:74666000-74666800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr15:74666000-74666800	Active TSS	Primary T cells from cord blood	blood
10	chr15:74666000-74666800	Active TSS	Fetal Brain Female	brain
11	chr15:74666000-74667000	Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr15:74666000-74667000	Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr15:74666000-74667000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr15:74666000-74667000	Flanking Active TSS	Primary B cells from cord blood	blood
15	chr15:74666000-74667000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr15:74666000-74667000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr15:74666000-74667000	Active TSS	Brain Hippocampus Middle	brain
18	chr15:74666000-74667000	Active TSS	Esophagus	oesophagus
19	chr15:74666000-74667000	Active TSS	A549	lung
20	chr15:74666000-74667000	Active TSS	Osteobl	bone
21	chr15:74666000-74667200	Active TSS	H9 Cell Line	embryonic stem cell
22	chr15:74666000-74667200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr15:74666000-74667200	Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr15:74666000-74667200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
25	chr15:74666000-74667200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
26	chr15:74666000-74667200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr15:74666000-74667200	Flanking Active TSS	Duodenum Mucosa	Duodenum
28	chr15:74666000-74667200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
29	chr15:74666000-74667200	Flanking Active TSS	Dnd41	blood
30	chr15:74666000-74667200	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
31	chr15:74666000-74667200	Flanking Active TSS	NH-A	brain
32	chr15:74666000-74667400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr15:74666000-74667600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
34	chr15:74666000-74667600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr15:74666000-74667600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr15:74666000-74667600	Flanking Active TSS	Stomach Smooth Muscle	stomach
37	chr15:74666000-74667600	Flanking Active TSS	HMEC	breast
38	chr15:74666200-74666800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr15:74666200-74666800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr15:74666200-74666800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr15:74666200-74666800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr15:74666200-74666800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr15:74666200-74666800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr15:74666200-74666800	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
45	chr15:74666200-74666800	Flanking Active TSS	Primary hematopoietic stem cells	blood
46	chr15:74666200-74666800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
47	chr15:74666200-74666800	Active TSS	Primary T killer memory cells from peripheral blood	blood
48	chr15:74666200-74666800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr15:74666200-74666800	Active TSS	Aorta	Aorta
50	chr15:74666200-74666800	Active TSS	Brain Angular Gyrus	brain

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