Variant report

Variant	rs60358948
Chromosome Location	chr15:35254467-35254468
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:35252403..35254603-chr15:35260374..35262627,3	K562	blood:
2	chr15:35251304..35254918-chr15:35255503..35258833,5	K562	blood:
3	chr15:35252626..35258121-chr15:35259367..35263228,9	K562	blood:
4	chr15:34875842..34878722-chr15:35253845..35256501,2	K562	blood:

Variant related genes	Relation type
ENSG00000021776	Chromatin interaction
ENSG00000215252	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10163053	0.93[EUR][1000 genomes]
rs10163067	0.93[EUR][1000 genomes]
rs11854422	1.00[ASN][1000 genomes]
rs12324241	1.00[ASN][1000 genomes]
rs16954283	1.00[ASN][1000 genomes]
rs16960205	0.96[AFR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16960207	0.96[AFR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16960208	0.96[AFR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16973797	0.93[EUR][1000 genomes]
rs17237242	1.00[ASN][1000 genomes]
rs17237249	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17415658	1.00[ASN][1000 genomes]
rs17818176	1.00[ASN][1000 genomes]
rs17818182	0.83[ASN][1000 genomes]
rs2293125	1.00[ASN][1000 genomes]
rs28392765	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs28393184	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28444764	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6495719	1.00[ASN][1000 genomes]
rs7171890	1.00[ASN][1000 genomes]
rs7174356	1.00[ASN][1000 genomes]
rs7180251	0.93[EUR][1000 genomes]
rs74008016	0.93[EUR][1000 genomes]
rs74008018	0.93[EUR][1000 genomes]
rs9972346	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3350109	chr15:34668106-35534229	Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv522411	chr15:34953986-35462981	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	esv2761865	chr15:35101678-35271639	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv832967	chr15:35110102-35267906	Strong transcription Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv904072	chr15:35150897-35259376	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv569154	chr15:35165366-35259376	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	7 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	chr15:35198800-35261200	Weak transcription	Esophagus	oesophagus
2	chr15:35207000-35259400	Weak transcription	Small Intestine	intestine
3	chr15:35220600-35260200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:35221200-35260800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr15:35223400-35260600	Weak transcription	Fetal Heart	heart
6	chr15:35224200-35258800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr15:35225400-35259200	Weak transcription	Psoas Muscle	Psoas
8	chr15:35229400-35261000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr15:35232200-35260800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr15:35232400-35256600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr15:35232800-35258800	Weak transcription	Brain Germinal Matrix	brain
12	chr15:35233200-35259600	Weak transcription	Brain Angular Gyrus	brain
13	chr15:35235000-35256400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr15:35235000-35256400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr15:35235000-35258000	Weak transcription	Brain Substantia Nigra	brain
16	chr15:35235000-35258800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr15:35235000-35260200	Weak transcription	Stomach Mucosa	stomach
18	chr15:35235000-35260800	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr15:35235200-35260800	Weak transcription	Fetal Brain Female	brain
20	chr15:35235400-35259400	Weak transcription	Gastric	stomach
21	chr15:35236600-35260800	Weak transcription	Fetal Kidney	kidney
22	chr15:35237400-35258600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr15:35239600-35257200	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr15:35240000-35261000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr15:35240600-35260600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr15:35240600-35260800	Weak transcription	Brain Anterior Caudate	brain
27	chr15:35243200-35261200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr15:35244600-35255000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr15:35244600-35259400	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr15:35244600-35259600	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr15:35244600-35260800	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr15:35244800-35260400	Weak transcription	HMEC	breast
33	chr15:35244800-35260800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr15:35244800-35260800	Weak transcription	Rectal Smooth Muscle	rectum
35	chr15:35245000-35260800	Weak transcription	NHDF-Ad	bronchial
36	chr15:35247400-35257400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr15:35248000-35259400	Weak transcription	Stomach Smooth Muscle	stomach
38	chr15:35248400-35260600	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr15:35248400-35260800	Weak transcription	Osteobl	bone
40	chr15:35248800-35259800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr15:35248800-35260200	Weak transcription	Pancreas	Pancrea
42	chr15:35249400-35259400	Weak transcription	Right Atrium	heart
43	chr15:35250200-35259800	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr15:35250400-35254600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr15:35250400-35255600	Strong transcription	Primary T helper cells fromperipheralblood	blood
46	chr15:35250400-35255600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr15:35250400-35255600	Strong transcription	Fetal Muscle Trunk	muscle
48	chr15:35250400-35256200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr15:35250400-35256600	Strong transcription	Primary B cells from peripheral blood	blood
50	chr15:35250400-35256800	Strong transcription	HUES6 Cell Line	embryonic stem cell

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