Variant report

Variant	rs28362900
Chromosome Location	chr15:74712947-74712948
allele	C/T
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:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:74692322..74695920-chr15:74711238..74714934,4	K562	blood:
2	chr15:74710597..74712982-chr15:75051460..75053643,2	K562	blood:
3	chr15:74711559..74715833-chr15:74724252..74727151,6	K562	blood:
4	chr15:74712461..74714565-chr15:74744762..74746348,2	MCF-7	breast:
5	chr15:74689719..74694435-chr15:74706184..74713253,9	MCF-7	breast:
6	chr15:74711706..74714244-chr15:74719320..74721195,2	K562	blood:
7	chr15:74698938..74701316-chr15:74711313..74715118,3	MCF-7	breast:
8	chr15:74680306..74681854-chr15:74712615..74715350,2	MCF-7	breast:
9	chr15:74674587..74678748-chr15:74711681..74714409,4	K562	blood:
10	chr15:74693785..74695419-chr15:74712435..74714990,2	MCF-7	breast:
11	chr15:74712355..74714244-chr15:74719225..74721195,3	K562	blood:
12	chr15:74675641..74677310-chr15:74711681..74714409,2	K562	blood:
13	chr15:74712692..74714612-chr15:74714775..74716965,2	MCF-7	breast:
14	chr15:74710571..74713498-chr15:74715208..74717540,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000138623	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11852760	0.83[AFR][1000 genomes]
rs11855262	0.94[AFR][1000 genomes]
rs11858456	0.94[AFR][1000 genomes]
rs16968740	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28362873	1.00[ASN][1000 genomes]
rs28362880	0.94[AFR][1000 genomes]
rs28362884	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28362896	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28362897	1.00[ASN][1000 genomes]
rs28362907	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28362922	0.87[ASN][1000 genomes]
rs74023499	0.87[ASN][1000 genomes]
rs8023274	0.96[AFR][1000 genomes]
rs8031284	0.94[AFR][1000 genomes]
rs8042206	0.96[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 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	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
4	nsv904353	chr15:74697084-74716609	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
5	nsv904354	chr15:74697084-74722924	Enhancers Genic enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
6	nsv904355	chr15:74697084-74728149	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases
7	nsv904356	chr15:74697084-74729603	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases
8	nsv569974	chr15:74701200-74727113	Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases
9	nsv904357	chr15:74707993-74716609	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
10	nsv904358	chr15:74708461-74716609	Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
11	nsv569976	chr15:74709071-74715211	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Weak transcription Bivalent Enhancer	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
12	nsv904360	chr15:74709071-74728149	Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
13	nsv569979	chr15:74709405-74722924	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
14	nsv904363	chr15:74709975-74713279	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
15	nsv904364	chr15:74709975-74728149	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
16	nsv904366	chr15:74710125-74716609	Genic enhancers Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
17	nsv569982	chr15:74710125-74721969	Genic enhancers Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
18	nsv904367	chr15:74710125-74728149	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
19	nsv904368	chr15:74711122-74728149	Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74699600-74716600	Weak transcription	Fetal Kidney	kidney
2	chr15:74700000-74713800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr15:74701200-74714600	Genic enhancers	Spleen	Spleen
4	chr15:74702200-74715000	Weak transcription	Colonic Mucosa	Colon
5	chr15:74703200-74713000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr15:74703800-74713000	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr15:74706200-74713600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr15:74706400-74714600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr15:74706800-74715000	Weak transcription	Aorta	Aorta
10	chr15:74707200-74722400	Weak transcription	Fetal Intestine Small	intestine
11	chr15:74707800-74718000	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr15:74708000-74717600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr15:74708400-74722400	Genic enhancers	Fetal Thymus	thymus
14	chr15:74709000-74713000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr15:74709000-74715400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr15:74709000-74717600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr15:74709200-74720200	Weak transcription	Esophagus	oesophagus
18	chr15:74709200-74720800	Weak transcription	Primary hematopoietic stem cells	blood
19	chr15:74709200-74724800	Weak transcription	Primary T cells from cord blood	blood
20	chr15:74709400-74713800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr15:74709400-74713800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr15:74709400-74716000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr15:74709400-74718000	Enhancers	HSMMtube	muscle
24	chr15:74709600-74714400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr15:74709600-74718200	Enhancers	HMEC	breast
26	chr15:74709800-74713200	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr15:74709800-74718000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr15:74710000-74722800	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr15:74710200-74714800	Enhancers	Brain Angular Gyrus	brain
30	chr15:74710200-74718200	Enhancers	NHDF-Ad	bronchial
31	chr15:74710200-74718400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr15:74710200-74722000	Weak transcription	Dnd41	blood
33	chr15:74710400-74713600	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr15:74710400-74714000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr15:74710400-74714000	Weak transcription	Lung	lung
36	chr15:74710400-74714400	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr15:74710400-74716400	Enhancers	Brain Cingulate Gyrus	brain
38	chr15:74710400-74718200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr15:74710400-74721200	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr15:74710400-74722800	Enhancers	Brain Hippocampus Middle	brain
41	chr15:74710600-74714400	Weak transcription	Primary B cells from cord blood	blood
42	chr15:74711000-74718400	Enhancers	Brain Anterior Caudate	brain
43	chr15:74711000-74721000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr15:74711000-74723200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr15:74711000-74723400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr15:74711400-74713200	Enhancers	A549	lung
47	chr15:74711400-74713800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr15:74711400-74716400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr15:74711400-74717000	Enhancers	Fetal Brain Female	brain
50	chr15:74711400-74717600	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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