Variant report

Variant	rs7681714
Chromosome Location	chr4:56950938-56950939
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:56944085..56946867-chr4:56949220..56951165,2	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10517367	0.84[EUR][1000 genomes]
rs1108947	0.96[AFR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1108948	0.96[AFR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11721368	0.93[ASN][1000 genomes]
rs11729231	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11934389	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13102087	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13109242	0.86[ASN][1000 genomes]
rs13112752	0.83[EUR][1000 genomes]
rs13113844	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13121092	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13139132	0.82[ASN][1000 genomes]
rs13147381	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2412717	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2412718	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2412719	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2412720	0.83[EUR][1000 genomes]
rs2412722	0.84[EUR][1000 genomes]
rs2412723	0.95[ASN][1000 genomes]
rs34181414	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34546346	0.87[EUR][1000 genomes]
rs34577487	0.81[EUR][1000 genomes]
rs34683632	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34796075	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35204688	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35400594	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35417087	0.88[ASN][1000 genomes]
rs35770075	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35786306	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35786805	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs36092812	0.86[EUR][1000 genomes]
rs4355456	0.81[EUR][1000 genomes]
rs4364320	0.96[AFR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4645275	0.81[EUR][1000 genomes]
rs58795379	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58927874	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6554328	0.95[AFR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6839220	0.95[AFR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs71601617	0.93[ASN][1000 genomes]
rs73155601	0.81[EUR][1000 genomes]
rs7657181	0.96[AFR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7659294	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7659694	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7661471	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7663270	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7685766	0.85[EUR][1000 genomes];0.98[ASN][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	esv2755990	chr4:56317136-57143037	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	nsv1005845	chr4:56522075-56980357	Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv999328	chr4:56942917-57041586	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1007114	chr4:56942917-57055381	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv999639	chr4:56942917-57401310	Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	nsv1014045	chr4:56942917-57404511	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56944200-56951000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:56945200-56951800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:56945400-56951000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:56945400-56952200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:56945600-56965200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr4:56947000-56951800	Weak transcription	Fetal Intestine Small	intestine
7	chr4:56947200-56951600	Weak transcription	Duodenum Mucosa	Duodenum
8	chr4:56947600-56952200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr4:56947800-56957000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr4:56948800-56951200	Weak transcription	Ovary	ovary
11	chr4:56948800-56972200	Weak transcription	Fetal Stomach	stomach
12	chr4:56949000-56951000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr4:56949000-56965200	Weak transcription	Primary hematopoietic stem cells	blood
14	chr4:56949600-56951000	Weak transcription	Brain Germinal Matrix	brain
15	chr4:56949600-56951400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr4:56949600-56951400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:56949600-56952200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr4:56950200-56951200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr4:56950800-56951200	Enhancers	Hela-S3	cervix
20	chr4:56950800-56951400	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr4:56950800-56952800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:56950800-56952800	Enhancers	Cortex derived primary cultured neurospheres	brain

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