Variant report

Variant	rs231591
Chromosome Location	chr19:36224705-36224706
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:21 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:36224087-36224905	K562	blood:	n/a	n/a
2	POLR2A	chr19:36224164-36224962	GM12878	blood:	n/a	n/a
3	POLR2A	chr19:36224216-36225586	GM12891	blood:	n/a	n/a
4	POLR2A	chr19:36223677-36224945	K562	blood:	n/a	n/a
5	POLR2A	chr19:36224218-36226771	GM12878	blood:	n/a	n/a
6	POLR2A	chr19:36224586-36224918	H1-hESC	embryonic stem cell:	n/a	n/a
7	POLR2A	chr19:36224206-36226701	GM12892	blood:	n/a	n/a
8	POLR2A	chr19:36224043-36224864	A549	lung:	n/a	n/a
9	POLR2A	chr19:36224219-36224858	PANC-1	pancreas:	n/a	n/a
10	POLR2A	chr19:36224281-36224738	GM12891	blood:	n/a	n/a
11	POLR2A	chr19:36224195-36224823	GM12892	blood:	n/a	n/a
12	POLR2A	chr19:36223791-36224822	GM12878	blood:	n/a	n/a
13	POLR2A	chr19:36224209-36226045	GM12891	blood:	n/a	n/a
14	POLR2A	chr19:36224239-36224911	SK-N-MC	brain:	n/a	n/a
15	POLR2A	chr19:36224029-36224707	PFSK-1	brain:	n/a	n/a
16	POLR2A	chr19:36223820-36225481	K562	blood:	n/a	n/a
17	POLR2A	chr19:36224320-36226298	A549	lung:	n/a	n/a
18	ZNF263	chr19:36224535-36224819	HEK293-T-REx	kidney:	n/a	n/a
19	POLR2A	chr19:36224677-36225093	U87	brain:	n/a	n/a
20	POLR2A	chr19:36224273-36225148	HepG2	liver:	n/a	n/a
21	POLR2A	chr19:36224581-36224816	GM12878	blood:	n/a	n/a

No data

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:36223600..36226210-chr19:36262533..36266105,3	K562	blood:
2	chr19:36223134..36225733-chr19:36234939..36237543,2	MCF-7	breast:

No data

Variant related genes	Relation type
KMT2B	TF binding region
ENSG00000267120	Chromatin interaction
ENSG00000004777	Chromatin interaction
ENSG00000205155	Chromatin interaction
ENSG00000188223	Chromatin interaction
ENSG00000161265	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 8 )

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

rs_ID	r²[population]
rs107068	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1269214	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs173003	0.82[CEU][hapmap];0.86[EUR][1000 genomes]
rs179570	1.00[CEU][hapmap];0.83[CHB][hapmap];0.91[JPT][hapmap];0.80[YRI][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2242522	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2242523	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2285421	0.85[CEU][hapmap]
rs231238	1.00[CEU][hapmap];0.83[CHB][hapmap];0.91[JPT][hapmap];0.80[YRI][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs231244	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs231588	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs231592	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55939240	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs614225	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs807478	0.85[EUR][1000 genomes]
rs807479	1.00[CEU][hapmap];0.83[CHB][hapmap];0.91[JPT][hapmap];0.80[YRI][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9917056	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432045	chr19:35556260-36520760	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv911630	chr19:36149761-36290977	Enhancers Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	69 gene(s)	inside rSNPs	diseases
3	nsv458566	chr19:36156588-36265508	Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
4	nsv579422	chr19:36156588-36265508	Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
5	nsv911631	chr19:36169285-36290977	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
6	nsv911632	chr19:36174176-36288297	Strong transcription Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
7	nsv911633	chr19:36206050-36283847	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
8	nsv911634	chr19:36206050-36290977	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
9	nsv543996	chr19:36210269-36265431	Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
10	nsv1057830	chr19:36210269-36279794	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
11	nsv543997	chr19:36210269-36279794	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
12	nsv911635	chr19:36217333-36283847	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
13	nsv515536	chr19:36219525-36240960	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
14	nsv458567	chr19:36221051-36283847	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
15	nsv579423	chr19:36221051-36283847	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs231591	ZBTB32	cis	Nerve Tibial	GTEx
rs231591	AC002398.13	cis	Thyroid	GTEx
rs231591	ZBTB32	cis	Thyroid	GTEx
rs231591	RN7SL765P	cis	Muscle Skeletal	GTEx
rs231591	COX6B1	cis	Heart Left Ventricle	GTEx
rs231591	TMEM149	Cis_1M	lymphoblastoid	RTeQTL
rs231591	ZBTB32	cis	lung	GTEx
rs231591	COX6B1	cis	Muscle Skeletal	GTEx

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36210600-36230000	Strong transcription	HUES64 Cell Line	embryonic stem cell
2	chr19:36210600-36230200	Strong transcription	HUES6 Cell Line	embryonic stem cell
3	chr19:36210600-36230200	Strong transcription	Cortex derived primary cultured neurospheres	brain
4	chr19:36210600-36230200	Strong transcription	Ovary	ovary
5	chr19:36210600-36230200	Strong transcription	Sigmoid Colon	Sigmoid Colon
6	chr19:36210600-36230400	Strong transcription	Brain Inferior Temporal Lobe	brain
7	chr19:36210600-36230400	Strong transcription	A549	lung
8	chr19:36210600-36230600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr19:36210600-36230600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr19:36210600-36230600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr19:36210600-36230600	Weak transcription	Right Atrium	heart
12	chr19:36210600-36230600	Strong transcription	NHLF	lung
13	chr19:36210600-36231200	Weak transcription	Fetal Brain Male	brain
14	chr19:36210800-36225000	Strong transcription	Fetal Muscle Trunk	muscle
15	chr19:36210800-36227400	Strong transcription	Primary B cells from peripheral blood	blood
16	chr19:36210800-36228000	Strong transcription	Fetal Thymus	thymus
17	chr19:36210800-36229600	Strong transcription	H1 Cell Line	embryonic stem cell
18	chr19:36210800-36229800	Strong transcription	Adipose Nuclei	Adipose
19	chr19:36210800-36230000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr19:36210800-36230200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr19:36210800-36230200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr19:36210800-36230200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr19:36210800-36230200	Strong transcription	Fetal Intestine Large	intestine
24	chr19:36210800-36230200	Strong transcription	Gastric	stomach
25	chr19:36210800-36230200	Strong transcription	Thymus	Thymus
26	chr19:36210800-36230400	Strong transcription	H9 Cell Line	embryonic stem cell
27	chr19:36210800-36230400	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr19:36210800-36230400	Strong transcription	Primary neutrophils fromperipheralblood	blood
29	chr19:36210800-36230400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr19:36210800-36230400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr19:36210800-36230400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr19:36210800-36230400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr19:36210800-36230400	Strong transcription	Brain Cingulate Gyrus	brain
34	chr19:36210800-36230400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr19:36210800-36230400	Strong transcription	Colonic Mucosa	Colon
36	chr19:36210800-36230600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr19:36210800-36231000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr19:36211000-36225200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr19:36211000-36227600	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr19:36211000-36230000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
41	chr19:36211000-36230000	Strong transcription	Left Ventricle	heart
42	chr19:36211000-36230200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr19:36211000-36230200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr19:36211000-36230200	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr19:36211000-36230200	Strong transcription	Osteobl	bone
46	chr19:36211000-36230400	Strong transcription	HUES48 Cell Line	embryonic stem cell
47	chr19:36211000-36230400	Strong transcription	Muscle Satellite Cultured Cells	--
48	chr19:36211000-36230400	Strong transcription	Fetal Muscle Leg	muscle
49	chr19:36211000-36230400	Strong transcription	Lung	lung
50	chr19:36211000-36230600	Strong transcription	iPS-15b Cell Line	embryonic stem cell

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