Variant report

Variant	rs34854082
Chromosome Location	chr1:113586927-113586928
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:113421587..113424736-chr1:113583992..113587746,3	K562	blood:
2	chr1:113490213..113492007-chr1:113585398..113587870,2	K562	blood:
3	chr1:113585683..113588057-chr1:113615686..113617260,2	K562	blood:
4	chr1:113582365..113584393-chr1:113584924..113587944,3	K562	blood:
5	chr1:113577576..113579367-chr1:113585664..113588475,2	K562	blood:
6	chr1:113498071..113501633-chr1:113584474..113587906,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000238198	Chromatin interaction
ENSG00000226419	Chromatin interaction
ENSG00000155380	Chromatin interaction
ENSG00000198799	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10494148	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10494149	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10494150	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11102590	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12070586	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12072108	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12073607	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12125253	0.83[AMR][1000 genomes]
rs12129924	0.81[AMR][1000 genomes]
rs12139041	0.85[AFR][1000 genomes]
rs12141890	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12732564	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12748429	0.81[AMR][1000 genomes]
rs12757593	0.82[EUR][1000 genomes]
rs1316767	0.81[AMR][1000 genomes]
rs1661	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17031099	0.82[EUR][1000 genomes]
rs34236373	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35793987	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4240536	0.81[EUR][1000 genomes]
rs4630126	0.81[EUR][1000 genomes]
rs56204018	0.81[EUR][1000 genomes]
rs72683494	0.84[EUR][1000 genomes]
rs72685622	0.81[EUR][1000 genomes]
rs749956	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7543653	0.82[EUR][1000 genomes]
rs7548091	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7551138	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7556148	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002971	chr1:112924725-113740584	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
2	nsv535059	chr1:112924725-113740584	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
3	nsv1010276	chr1:113123932-113740584	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
4	nsv533295	chr1:113167645-113589588	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
5	nsv1012119	chr1:113214869-113759081	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
6	nsv535060	chr1:113214869-113759081	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
7	nsv529238	chr1:113229946-113759080	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
8	nsv997426	chr1:113288282-113639507	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer 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	68 gene(s)	inside rSNPs	diseases
9	nsv999915	chr1:113360145-113684833	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
10	esv18293	chr1:113375437-113852815	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
11	nsv1007045	chr1:113425222-113839910	Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer 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	59 gene(s)	inside rSNPs	diseases
12	nsv946146	chr1:113567302-113640814	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
13	nsv427719	chr1:113570229-114078388	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:113580200-113589200	Weak transcription	Right Atrium	heart
2	chr1:113582600-113587400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:113582800-113587600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr1:113584400-113587000	Enhancers	Fetal Thymus	thymus
5	chr1:113584800-113589400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr1:113585000-113591000	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr1:113585200-113588000	Enhancers	H1 Cell Line	embryonic stem cell
8	chr1:113585400-113588800	Weak transcription	Primary T cells from cord blood	blood
9	chr1:113585400-113588800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr1:113585400-113588800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr1:113585400-113589200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr1:113585600-113587800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr1:113585600-113588400	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr1:113585600-113588800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr1:113585600-113588800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr1:113585600-113599200	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr1:113585600-113601800	Weak transcription	Fetal Stomach	stomach
18	chr1:113585800-113587400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr1:113585800-113587600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr1:113585800-113587600	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr1:113585800-113587800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr1:113585800-113588000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr1:113585800-113588800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr1:113585800-113588800	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr1:113585800-113588800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr1:113586000-113587600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr1:113586000-113588000	Enhancers	Rectal Mucosa Donor 29	rectum
28	chr1:113586000-113588400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr1:113586000-113588800	Weak transcription	Primary B cells from cord blood	blood
30	chr1:113586000-113589000	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr1:113586000-113589200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr1:113586200-113587800	Enhancers	H9 Cell Line	embryonic stem cell
33	chr1:113586200-113588800	Weak transcription	Primary hematopoietic stem cells	blood
34	chr1:113586200-113589200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:113586600-113587400	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr1:113586600-113587800	Weak transcription	Dnd41	blood
37	chr1:113586600-113588000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr1:113586600-113588000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr1:113586600-113588000	Enhancers	Adipose Nuclei	Adipose
40	chr1:113586600-113588800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr1:113586600-113588800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr1:113586600-113589200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr1:113586600-113589200	Weak transcription	Duodenum Mucosa	Duodenum
44	chr1:113586600-113589200	Weak transcription	K562	blood
45	chr1:113586600-113599600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr1:113586800-113587000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:113586800-113587200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr1:113586800-113587400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr1:113586800-113589200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:113586800-113589200	Weak transcription	GM12878-XiMat	blood

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