Variant report

Variant	rs534186
Chromosome Location	chr1:212636985-212636986
allele	C/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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:212636838..212639720-chr1:212643460..212645324,2	K562	blood:
2	chr1:212635707..212638056-chr1:212640059..212642694,3	K562	blood:
3	chr1:212230913..212233313-chr1:212635726..212638248,2	K562	blood:
4	chr1:212632904..212637583-chr1:212637604..212642982,9	K562	blood:
5	chr1:212635848..212638507-chr1:212642034..212643626,2	MCF-7	breast:
6	chr1:212626698..212637479-chr1:212779685..212784714,19	K562	blood:
7	chr1:212634664..212637460-chr1:212638255..212640310,2	MCF-7	breast:
8	chr1:212634967..212638975-chr1:212780720..212784132,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000162772	Chromatin interaction
ENSG00000224535	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs3767871	0.86[ASN][1000 genomes]
rs472463	0.84[ASN][1000 genomes]
rs479564	0.93[ASN][1000 genomes]
rs479807	0.85[ASN][1000 genomes]
rs4804	0.86[ASN][1000 genomes]
rs508432	0.86[ASN][1000 genomes]
rs514362	0.90[ASN][1000 genomes]
rs521469	0.86[ASN][1000 genomes]
rs527840	0.86[ASN][1000 genomes]
rs575025	0.91[ASN][1000 genomes]
rs577671	0.91[ASN][1000 genomes]
rs583058	0.86[ASN][1000 genomes]
rs595066	0.86[ASN][1000 genomes]
rs676490	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs681005	0.91[ASN][1000 genomes]
rs694274	0.91[ASN][1000 genomes]
rs791721	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009376	chr1:212292357-212680320	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv549139	chr1:212332294-212876902	Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
3	nsv997629	chr1:212404489-212658785	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	nsv535286	chr1:212404489-212658785	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
5	nsv1013110	chr1:212555764-212948092	Flanking Active TSS Bivalent/Poised TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	81 gene(s)	inside rSNPs	diseases
6	nsv535287	chr1:212555764-212948092	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	81 gene(s)	inside rSNPs	diseases
7	nsv873156	chr1:212585092-212646225	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
8	nsv873157	chr1:212610755-212640982	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv873158	chr1:212610755-212646225	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv873159	chr1:212610755-212669475	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv873160	chr1:212610755-212675482	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	nsv873161	chr1:212610755-212683565	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
13	nsv873162	chr1:212610755-212716033	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
14	nsv527863	chr1:212617423-212700618	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
15	nsv873163	chr1:212629935-212669475	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
16	nsv519924	chr1:212631393-212638725	Weak transcription Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212629800-212640000	Weak transcription	Pancreas	Pancrea
2	chr1:212629800-212642600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr1:212629800-212643200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr1:212632200-212637400	Enhancers	Brain Cingulate Gyrus	brain
5	chr1:212632200-212637400	Enhancers	Brain Hippocampus Middle	brain
6	chr1:212632800-212637000	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr1:212633400-212637000	Enhancers	Brain Anterior Caudate	brain
8	chr1:212634200-212637600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:212634400-212637000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr1:212635400-212638800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:212635600-212641800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:212635800-212637200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:212635800-212640600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr1:212635800-212641400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr1:212636200-212638200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr1:212636400-212637400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
17	chr1:212636400-212638400	Enhancers	Fetal Intestine Small	intestine
18	chr1:212636400-212641000	Weak transcription	Brain Angular Gyrus	brain
19	chr1:212636600-212637600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr1:212636600-212643200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr1:212636800-212637000	Bivalent Enhancer	HepG2	liver
22	chr1:212636800-212637200	Enhancers	H1 Cell Line	embryonic stem cell
23	chr1:212636800-212637200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:212636800-212637200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr1:212636800-212637400	Enhancers	Fetal Muscle Leg	muscle
26	chr1:212636800-212638600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr1:212636800-212638600	Enhancers	Fetal Intestine Large	intestine
28	chr1:212636800-212639800	Weak transcription	Brain Substantia Nigra	brain
29	chr1:212636800-212641600	Enhancers	Placenta Amnion	Placenta Amnion
30	chr1:212636800-212644400	Enhancers	Placenta	Placenta

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