Variant report

Variant	rs1197692
Chromosome Location	chr15:42175507-42175508
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:42175250..42178134-chr15:42183992..42185929,2	K562	blood:

Variant related genes	Relation type
ENSG00000174171	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1197657	0.85[ASN][1000 genomes]
rs1197658	0.85[ASN][1000 genomes]
rs1197683	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1197685	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1197694	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1197697	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1197700	1.00[ASN][1000 genomes]
rs1201690	1.00[ASN][1000 genomes]
rs1210795	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1211289	0.92[ASN][1000 genomes]
rs1704380	0.84[ASN][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	nsv931223	chr15:41989960-42781757	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
2	nsv427958	chr15:42051317-42301283	Strong transcription Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv904116	chr15:42076387-42229852	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
4	nsv1038393	chr15:42083574-42188035	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer 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
5	esv1827003	chr15:42087505-42199076	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS 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
6	nsv1041645	chr15:42095168-42186482	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
7	nsv1051200	chr15:42095168-42188035	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
8	nsv517631	chr15:42096926-42187492	Strong transcription Weak transcription Bivalent/Poised TSS Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
9	nsv1051733	chr15:42098896-42186482	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
10	nsv1036153	chr15:42098896-42188035	Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
11	nsv1035998	chr15:42098896-42434254	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
12	nsv1048606	chr15:42101694-42192760	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
13	nsv904117	chr15:42103822-42184794	Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
14	nsv904118	chr15:42103822-42207905	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
15	nsv904124	chr15:42109975-42207905	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
16	nsv9244	chr15:42110712-42208805	Enhancers Genic enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
17	nsv904125	chr15:42119900-42210393	Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Enhancers 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	19 gene(s)	inside rSNPs	diseases
18	nsv1050892	chr15:42128855-42186482	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
19	nsv1038933	chr15:42138456-42309087	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	30 gene(s)	inside rSNPs	diseases
20	nsv904127	chr15:42142912-42207905	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
21	nsv904128	chr15:42147639-42207905	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
22	nsv529687	chr15:42157320-42621682	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
23	nsv904129	chr15:42162957-42207905	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
24	esv3325887	chr15:42173185-42176033	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
25	esv3389238	chr15:42173510-42175708	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42141200-42191200	Weak transcription	Aorta	Aorta
2	chr15:42157400-42179200	Weak transcription	HSMMtube	muscle
3	chr15:42165400-42184800	Weak transcription	HMEC	breast
4	chr15:42172000-42178400	Enhancers	Liver	Liver
5	chr15:42172600-42175800	Strong transcription	HUVEC	blood vessel
6	chr15:42173600-42175800	Enhancers	Fetal Heart	heart
7	chr15:42173600-42175800	Enhancers	Spleen	Spleen
8	chr15:42173800-42175800	Enhancers	Left Ventricle	heart
9	chr15:42173800-42176000	Enhancers	Primary B cells from peripheral blood	blood
10	chr15:42173800-42176000	Enhancers	Primary hematopoietic stem cells	blood
11	chr15:42174000-42175800	Enhancers	Placenta Amnion	Placenta Amnion
12	chr15:42174000-42176000	Enhancers	Primary B cells from cord blood	blood
13	chr15:42174000-42180400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr15:42174000-42186000	Weak transcription	HSMM	muscle
15	chr15:42174200-42175600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr15:42174200-42175800	Enhancers	Brain Cingulate Gyrus	brain
17	chr15:42174200-42176000	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr15:42174200-42176000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr15:42174200-42186600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr15:42174400-42175600	Bivalent Enhancer	Fetal Thymus	thymus
21	chr15:42174400-42179400	Weak transcription	Lung	lung
22	chr15:42174800-42175600	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr15:42174800-42175600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr15:42174800-42175600	Enhancers	Gastric	stomach
25	chr15:42174800-42175800	Enhancers	Primary T cells from cord blood	blood
26	chr15:42174800-42176000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
27	chr15:42174800-42177000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr15:42174800-42180200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr15:42175000-42175600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
30	chr15:42175000-42175600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
31	chr15:42175000-42175600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr15:42175000-42175600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr15:42175000-42175600	Enhancers	Esophagus	oesophagus
34	chr15:42175000-42175600	Enhancers	Pancreas	Pancrea
35	chr15:42175000-42175600	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr15:42175000-42175800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr15:42175000-42175800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr15:42175000-42175800	Enhancers	Right Ventricle	heart
39	chr15:42175000-42176000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr15:42175000-42176000	Enhancers	Ovary	ovary
41	chr15:42175000-42180000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr15:42175000-42184600	Weak transcription	Right Atrium	heart
43	chr15:42175000-42186000	Weak transcription	Adipose Nuclei	Adipose
44	chr15:42175200-42175600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
45	chr15:42175200-42175600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr15:42175200-42175800	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr15:42175200-42176000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr15:42175400-42175600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr15:42175400-42175600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
50	chr15:42175400-42175800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle

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