Variant report

Variant	rs60337024
Chromosome Location	chr6:30576801-30576802
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:33)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:33 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:30576348-30586731	PANC-1	pancreas:	n/a	n/a
2	POLR2A	chr6:30576760-30578592	A549	lung:	n/a	n/a
3	POLR2A	chr6:30576514-30577456	ECC-1	luminal epithelium:	n/a	n/a
4	POLR2A	chr6:30576459-30586534	MCF10A-Er-Src	breast:	n/a	n/a
5	POLR2A	chr6:30576762-30586531	Hela-S3	cervix:	n/a	n/a
6	POLR2A	chr6:30576698-30576944	GM12878	blood:	n/a	n/a
7	POLR2A	chr6:30576660-30576874	GM12878	blood:	n/a	n/a
8	POLR2A	chr6:30576267-30586793	SK-N-MC	brain:	n/a	n/a
9	POLR2A	chr6:30576421-30586088	SK-N-SH	brain:	n/a	n/a
10	POLR2A	chr6:30576398-30576833	H1-neurons	neurons:	n/a	n/a
11	POLR2A	chr6:30576151-30586136	H1-hESC	embryonic stem cell:	n/a	n/a
12	POLR2A	chr6:30576533-30586585	GM12891	blood:	n/a	n/a
13	POLR2A	chr6:30576682-30576887	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr6:30576736-30576938	HepG2	liver:	n/a	n/a
15	POLR2A	chr6:30576601-30586578	GM12878	blood:	n/a	n/a
16	POLR2A	chr6:30576348-30586293	ECC-1	luminal epithelium:	n/a	n/a
17	POLR2A	chr6:30576768-30577121	HCT-116	colon:	n/a	n/a
18	POLR2A	chr6:30576712-30577284	HepG2	liver:	n/a	n/a
19	POLR2A	chr6:30576746-30576917	HUVEC	blood vessel:	n/a	n/a
20	POLR2A	chr6:30576539-30586508	MCF10A-Er-Src	breast:	n/a	n/a
21	POLR2A	chr6:30576787-30577252	ProgFib	skin:	n/a	n/a
22	POLR2A	chr6:30576353-30586641	PFSK-1	brain:	n/a	n/a
23	POLR2A	chr6:30576529-30586246	MCF-7	breast:	n/a	n/a
24	POLR2A	chr6:30576649-30578604	HepG2	liver:	n/a	n/a
25	POLR2A	chr6:30576404-30586729	PFSK-1	brain:	n/a	n/a
26	POLR2A	chr6:30575677-30585966	HepG2	liver:	n/a	n/a
27	POLR2A	chr6:30576695-30579733	K562	blood:	n/a	n/a
28	POLR2A	chr6:30576710-30577194	K562	blood:	n/a	n/a
29	POLR2A	chr6:30576485-30576829	K562	blood:	n/a	n/a
30	POLR2A	chr6:30576442-30579145	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr6:30576673-30586586	HepG2	liver:	n/a	n/a
32	POLR2A	chr6:30576678-30585977	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr6:30576540-30585908	K562	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105947026..105949255-chr6:30576466..30577973,2	MCF-7	breast:
2	chr6:30511109..30514018-chr6:30576685..30580337,3	MCF-7	breast:
3	chr1:26437641..26438529-chr6:30576426..30577256,2	Hela-S3	cervix:
4	chr6:30576582..30588788-chr6:30682721..30700088,114	K562	blood:
5	chr6:26123657..26124450-chr6:30576338..30576925,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
PPP1R10	TF binding region
ENSG00000272540	Chromatin interaction
ENSG00000196230	Chromatin interaction
ENSG00000180573	Chromatin interaction
ENSG00000175087	Chromatin interaction
ENSG00000180596	Chromatin interaction
ENSG00000137337	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs17189364	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17195551	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56212767	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60794866	0.91[AFR][1000 genomes]
rs73727439	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73727448	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73727449	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73727450	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73727451	0.98[AFR][1000 genomes]
rs73727466	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025667	chr6:30292845-30638066	Flanking Active TSS Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Enhancers 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 miRNA target site	825 gene(s)	inside rSNPs	diseases
2	esv3519970	chr6:30382942-31378788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
3	esv3519971	chr6:30382942-31378788	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
4	nsv601481	chr6:30422632-31284253	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1012 gene(s)	inside rSNPs	diseases
5	esv3430377	chr6:30443802-30814426	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	967 gene(s)	inside rSNPs	diseases
6	nsv884086	chr6:30462084-30672757	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	798 gene(s)	inside rSNPs	diseases
7	nsv884091	chr6:30526026-30590646	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	776 gene(s)	inside rSNPs	diseases
8	nsv5244	chr6:30545111-30589803	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers 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	772 gene(s)	inside rSNPs	diseases
9	nsv830626	chr6:30558064-30732905	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	406 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30540200-30582200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:30540200-30582200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:30542200-30581800	Weak transcription	Right Atrium	heart
4	chr6:30564200-30577400	Strong transcription	Fetal Intestine Small	intestine
5	chr6:30566400-30581000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr6:30566600-30578000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr6:30566600-30579600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
8	chr6:30566800-30577600	Strong transcription	Osteobl	bone
9	chr6:30566800-30578400	Strong transcription	Thymus	Thymus
10	chr6:30567000-30577800	Strong transcription	NH-A	brain
11	chr6:30567000-30579400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
12	chr6:30567000-30579600	Strong transcription	Fetal Muscle Trunk	muscle
13	chr6:30567200-30579600	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr6:30567400-30577800	Strong transcription	Muscle Satellite Cultured Cells	--
15	chr6:30567400-30578000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr6:30567400-30578000	Strong transcription	HSMM	muscle
17	chr6:30567400-30578200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr6:30567400-30578200	Strong transcription	Fetal Muscle Leg	muscle
19	chr6:30567400-30579000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr6:30567400-30579200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
21	chr6:30567400-30579800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:30567400-30580000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:30567400-30580200	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr6:30567400-30580400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
25	chr6:30567600-30577000	Strong transcription	Stomach Smooth Muscle	stomach
26	chr6:30567600-30578400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr6:30567600-30580400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr6:30568000-30577600	Strong transcription	Brain Inferior Temporal Lobe	brain
29	chr6:30568000-30577800	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr6:30568000-30578200	Strong transcription	Dnd41	blood
31	chr6:30568000-30580000	Strong transcription	HUES48 Cell Line	embryonic stem cell
32	chr6:30568000-30580200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr6:30568200-30577000	Strong transcription	Primary B cells from cord blood	blood
34	chr6:30568200-30577200	Strong transcription	Skeletal Muscle Female	skeletal muscle
35	chr6:30568200-30577400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr6:30568200-30577400	Strong transcription	Placenta Amnion	Placenta Amnion
37	chr6:30568200-30577400	Strong transcription	HMEC	breast
38	chr6:30568200-30577400	Strong transcription	HSMMtube	muscle
39	chr6:30568200-30577800	Strong transcription	Fetal Intestine Large	intestine
40	chr6:30568200-30578000	Strong transcription	Duodenum Mucosa	Duodenum
41	chr6:30568200-30579200	Strong transcription	H1 Cell Line	embryonic stem cell
42	chr6:30568200-30579600	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr6:30568200-30579800	Strong transcription	A549	lung
44	chr6:30568200-30579800	Strong transcription	NHEK	skin
45	chr6:30568400-30577000	Strong transcription	Primary B cells from peripheral blood	blood
46	chr6:30568400-30577000	Strong transcription	Adipose Nuclei	Adipose
47	chr6:30568400-30577200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr6:30568400-30577200	Strong transcription	Duodenum Smooth Muscle	Duodenum
49	chr6:30568400-30577200	Strong transcription	Gastric	stomach
50	chr6:30568400-30577200	Strong transcription	Skeletal Muscle Male	skeletal muscle

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