Variant report

Variant	rs2814978
Chromosome Location	chr6:34577776-34577777
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:34216569..34217473-chr6:34577039..34578066,5	K562	blood:
2	chr6:34131703..34132237-chr6:34577100..34577997,4	K562	blood:
3	chr6:34494469..34496151-chr6:34577655..34579267,2	K562	blood:
4	chr6:34570143..34573485-chr6:34575901..34578410,4	K562	blood:
5	chr6:34389543..34392332-chr6:34575346..34578264,2	K562	blood:
6	chr6:34163718..34164707-chr6:34577121..34577992,3	K562	blood:
7	chr6:34382616..34385085-chr6:34576008..34577878,2	K562	blood:
8	chr6:34433254..34436133-chr6:34577509..34579305,2	K562	blood:
9	chr6:34496704..34498115-chr6:34576145..34578099,12	MCF-7	breast:
10	chr6:34577643..34579830-chr6:34629436..34632092,2	K562	blood:
11	chr6:34498308..34501187-chr6:34577541..34579069,2	MCF-7	breast:
12	chr6:34494680..34495634-chr6:34577124..34578035,2	MCF-7	breast:
13	chr6:34023643..34024284-chr6:34577063..34577946,2	K562	blood:
14	chr6:34494608..34496228-chr6:34576974..34578003,14	K562	blood:
15	chr6:34496972..34497706-chr6:34576720..34577905,3	MCF-7	breast:
16	chr6:34389543..34394732-chr6:34574811..34579307,4	K562	blood:
17	chr6:34204562..34206491-chr6:34577432..34579117,2	K562	blood:
18	chr6:34360143..34362541-chr6:34575968..34579068,3	K562	blood:
19	chr6:34427357..34428310-chr6:34577023..34577948,4	K562	blood:
20	chr6:34503783..34506203-chr6:34577530..34580135,3	MCF-7	breast:
21	chr6:34359197..34361923-chr6:34576556..34579097,2	K562	blood:
22	chr6:34208449..34211320-chr6:34575823..34577812,2	K562	blood:
23	chr6:34559418..34564619-chr6:34574111..34579705,5	K562	blood:

No data

Variant related genes	Relation type
ENSG00000124614	Chromatin interaction
ENSG00000272325	Chromatin interaction
ENSG00000124493	Chromatin interaction
ENSG00000186577	Chromatin interaction
ENSG00000270800	Chromatin interaction
ENSG00000124507	Chromatin interaction
ENSG00000137309	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1201873	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1201874	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs188190	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs205258	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs205259	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs205260	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs205286	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2235568	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2235569	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2262245	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2395598	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2395599	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2744941	0.81[EUR][1000 genomes]
rs2744943	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2744949	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2744957	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2744959	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2744973	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2744974	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2814945	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2814972	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2814974	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2814975	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2814976	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2814979	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2814981	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2814984	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2814987	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2814988	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2814991	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2814992	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2814995	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2815001	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2815004	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs412392	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6937784	0.82[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	nsv1022844	chr6:34317219-35060519	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv538195	chr6:34317219-35060519	Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	esv2758046	chr6:34382492-34714677	Genic enhancers Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	esv2759418	chr6:34382492-34714677	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv885785	chr6:34404636-34874002	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	nsv1033583	chr6:34471572-34828372	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
7	nsv885792	chr6:34507311-34607958	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
8	nsv885793	chr6:34520267-34886436	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers 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 target site	47 gene(s)	inside rSNPs	diseases
9	nsv823667	chr6:34533015-34592524	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer 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 target site	14 gene(s)	inside rSNPs	diseases
10	nsv818410	chr6:34538544-34579431	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	12 gene(s)	inside rSNPs	diseases
11	nsv830640	chr6:34542489-34714677	Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
12	nsv885794	chr6:34561585-34673149	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
13	nsv1032557	chr6:34565802-34802008	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
14	nsv538196	chr6:34565802-34802008	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
15	esv2763967	chr6:34566255-34925463	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs2814978	UHRF1BP1	cis	Adipose Subcutaneous	GTEx
rs2814978	UHRF1BP1	cis	Nerve Tibial	GTEx
rs2814978	UHRF1BP1	cis	Artery Tibial	GTEx
rs2814978	C6orf107	Cis_1M	lymphoblastoid	RTeQTL
rs2814978	UHRF1BP1	cis	Muscle Skeletal	GTEx
rs2814978	UHRF1BP1	cis	Esophagus Muscularis	GTEx
rs2814978	UHRF1BP1	cis	lung	GTEx
rs2814978	UHRF1BP1	cis	Whole Blood	GTEx
rs2814978	UHRF1BP1	cis	Artery Aorta	GTEx
rs2814978	UHRF1BP1	cis	Stomach	GTEx
rs2814978	SNRPC	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34556200-34612200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr6:34557400-34612400	Weak transcription	Fetal Kidney	kidney
3	chr6:34560400-34578600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr6:34562600-34585200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:34563800-34579000	Weak transcription	HMEC	breast
6	chr6:34564000-34578000	Weak transcription	NHDF-Ad	bronchial
7	chr6:34567000-34612200	Weak transcription	Fetal Lung	lung
8	chr6:34567800-34612400	Weak transcription	Rectal Smooth Muscle	rectum
9	chr6:34569400-34583600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr6:34570400-34612600	Weak transcription	Brain Anterior Caudate	brain
11	chr6:34570600-34583600	Weak transcription	HSMMtube	muscle
12	chr6:34570600-34610000	Weak transcription	Brain Hippocampus Middle	brain
13	chr6:34570800-34578000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr6:34570800-34578600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr6:34570800-34579000	Weak transcription	HSMM	muscle
16	chr6:34570800-34579200	Weak transcription	NH-A	brain
17	chr6:34570800-34581800	Weak transcription	Brain Cingulate Gyrus	brain
18	chr6:34570800-34582000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr6:34570800-34584600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr6:34570800-34587000	Weak transcription	Brain Substantia Nigra	brain
21	chr6:34570800-34618800	Weak transcription	Brain Angular Gyrus	brain
22	chr6:34571000-34578600	Weak transcription	Psoas Muscle	Psoas
23	chr6:34571000-34578600	Weak transcription	Right Atrium	heart
24	chr6:34571000-34585200	Weak transcription	Right Ventricle	heart
25	chr6:34571000-34621400	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr6:34571000-34624000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr6:34571400-34578600	Weak transcription	Pancreas	Pancrea
28	chr6:34572000-34578000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr6:34572400-34578000	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr6:34572400-34612600	Weak transcription	Aorta	Aorta
31	chr6:34573800-34607200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr6:34574400-34584200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr6:34574400-34612400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr6:34574400-34623400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr6:34574600-34577800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr6:34574600-34578400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:34574600-34579800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr6:34574600-34579800	Weak transcription	Left Ventricle	heart
39	chr6:34574600-34581600	Weak transcription	Fetal Intestine Large	intestine
40	chr6:34574600-34583400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr6:34574600-34583400	Weak transcription	Spleen	Spleen
42	chr6:34574600-34583800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr6:34574600-34583800	Weak transcription	Thymus	Thymus
44	chr6:34574600-34585200	Weak transcription	Ovary	ovary
45	chr6:34574600-34598200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr6:34574600-34598200	Weak transcription	Lung	lung
47	chr6:34574600-34612600	Weak transcription	Gastric	stomach
48	chr6:34574600-34613600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr6:34574600-34613600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr6:34574800-34578000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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