Variant report

Variant	rs71337524
Chromosome Location	chr19:36528247-36528248
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GABPA	chr19:36527881-36528519	HL-60	blood:	n/a	n/a
2	POLR2A	chr19:36527938-36528480	HL-60	blood:	n/a	n/a
3	GABPA	chr19:36528015-36528475	HL-60	blood:	n/a	n/a
4	POLR2A	chr19:36527975-36528378	HepG2	liver:	n/a	n/a
5	SPI1	chr19:36527879-36528447	HL-60	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:36526205..36528558-chr19:36530375..36532258,2	K562	blood:

Variant related genes	Relation type
CLIP3	TF binding region

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10407011	0.82[EUR][1000 genomes]
rs10414877	0.84[EUR][1000 genomes]
rs10420353	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10421966	0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10423651	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10425692	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10426582	0.95[ASN][1000 genomes]
rs12462432	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12462632	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12462674	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12972490	0.85[AFR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12976505	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12976812	0.87[AFR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12977814	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12978482	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12979093	0.95[ASN][1000 genomes]
rs12981654	0.87[AFR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17639286	0.90[EUR][1000 genomes]
rs2023865	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2239510	0.82[EUR][1000 genomes]
rs34906485	0.88[ASN][1000 genomes]
rs35125548	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35875194	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3826995	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4461192	0.82[EUR][1000 genomes]
rs4805154	0.88[ASN][1000 genomes]
rs4805155	0.95[ASN][1000 genomes]
rs4806252	0.95[ASN][1000 genomes]
rs4806253	0.97[ASN][1000 genomes]
rs721542	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7250448	0.94[ASN][1000 genomes]
rs7259592	0.83[EUR][1000 genomes]
rs7260609	0.85[EUR][1000 genomes]
rs8103569	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[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	nsv911638	chr19:36265508-36537959	Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	esv3526489	chr19:36306483-36741945	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
3	esv3526490	chr19:36306483-36741945	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
4	esv1831737	chr19:36324324-36690874	Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
5	nsv911641	chr19:36473677-36536938	Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv833815	chr19:36519803-36624936	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36506400-36544400	Weak transcription	GM12878-XiMat	blood
2	chr19:36506800-36532400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr19:36507000-36532200	Weak transcription	Hela-S3	cervix
4	chr19:36508800-36532400	Weak transcription	NHEK	skin
5	chr19:36515400-36544600	Weak transcription	Pancreas	Pancrea
6	chr19:36516400-36532400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr19:36518800-36532200	Weak transcription	A549	lung
8	chr19:36524000-36529400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr19:36524000-36532000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr19:36524000-36532000	Weak transcription	Psoas Muscle	Psoas
11	chr19:36524000-36537000	Weak transcription	Small Intestine	intestine
12	chr19:36524200-36528400	Weak transcription	Right Ventricle	heart
13	chr19:36524200-36528600	Weak transcription	Adipose Nuclei	Adipose
14	chr19:36524200-36529800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr19:36524200-36530000	Weak transcription	Fetal Intestine Large	intestine
16	chr19:36524200-36530000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr19:36524200-36530200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr19:36524200-36530200	Weak transcription	Ovary	ovary
19	chr19:36524200-36530400	Weak transcription	Colonic Mucosa	Colon
20	chr19:36524200-36531600	Weak transcription	Placenta	Placenta
21	chr19:36524200-36532000	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr19:36524200-36532200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr19:36524200-36532200	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr19:36524200-36532200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr19:36524200-36532200	Weak transcription	NHLF	lung
26	chr19:36524200-36532400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr19:36524200-36532400	Weak transcription	HSMMtube	muscle
28	chr19:36524200-36533200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr19:36524200-36543800	Weak transcription	Left Ventricle	heart
30	chr19:36524200-36544000	Weak transcription	Primary B cells from cord blood	blood
31	chr19:36524200-36544400	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr19:36524200-36544400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr19:36524200-36544400	Weak transcription	Aorta	Aorta
34	chr19:36524400-36529000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr19:36524400-36529000	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr19:36524400-36529800	Weak transcription	Brain Hippocampus Middle	brain
37	chr19:36524400-36532200	Weak transcription	Fetal Kidney	kidney
38	chr19:36524400-36532200	Weak transcription	NHDF-Ad	bronchial
39	chr19:36524400-36532400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr19:36524400-36532400	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr19:36524400-36532400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr19:36524400-36532400	Weak transcription	Colon Smooth Muscle	Colon
43	chr19:36524400-36532400	Weak transcription	Rectal Smooth Muscle	rectum
44	chr19:36524400-36533000	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr19:36524400-36534800	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr19:36524400-36535000	Weak transcription	Brain Angular Gyrus	brain
47	chr19:36524400-36537200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr19:36524400-36537200	Weak transcription	Brain Cingulate Gyrus	brain
49	chr19:36524400-36543800	Weak transcription	Primary B cells from peripheral blood	blood
50	chr19:36524400-36544000	Weak transcription	Fetal Lung	lung

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