Variant report

Variant	rs61820082
Chromosome Location	chr1:221889694-221889695
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZNF263	chr1:221888754-221889768	HEK293-T-REx	kidney:	n/a	chr1:221889270-221889291
2	WRNIP1	chr1:221889555-221889755	GM12878	blood:	n/a	n/a
3	MAFK	chr1:221889691-221890024	HepG2	liver:	n/a	n/a
4	POLR2A	chr1:221888575-221894363	GM12891	blood:	n/a	n/a
5	POLR2A	chr1:221889427-221889926	GM12878	blood:	n/a	n/a
6	GATA1	chr1:221889490-221891216	K562	blood:	n/a	chr1:221890579-221890588 chr1:221890411-221890421

No.	Distal block	Cell Line	Cell type
1	chr1:221886064..221888475-chr1:221888570..221891136,3	K562	blood:
2	chr1:221889093..221891683-chr1:222160866..222163448,2	K562	blood:
3	chr1:221887650..221891571-chr1:221892438..221898117,9	K562	blood:
4	chr1:221882652..221891989-chr1:221912814..221917285,15	K562	blood:
5	chr1:221886657..221890286-chr1:221915663..221918002,3	MCF-7	breast:

Variant related genes	Relation type
DUSP10	TF binding region
ENSG00000143507	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs61820076	0.82[EUR][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	nsv469786	chr1:221855871-222040335	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv482867	chr1:221855871-222040335	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1002463	chr1:221863355-222095773	Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	nsv535302	chr1:221863355-222095773	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv1007092	chr1:221883491-221958279	Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	nsv535303	chr1:221883491-221958279	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221879600-221891000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr1:221879600-221891800	Enhancers	Fetal Thymus	thymus
3	chr1:221879600-221902400	Enhancers	Brain Substantia Nigra	brain
4	chr1:221879800-221890200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:221879800-221890200	Weak transcription	Fetal Muscle Trunk	muscle
6	chr1:221879800-221896800	Enhancers	Colon Smooth Muscle	Colon
7	chr1:221880400-221893200	Enhancers	Primary hematopoietic stem cells	blood
8	chr1:221882600-221893400	Enhancers	Brain Cingulate Gyrus	brain
9	chr1:221882800-221899000	Genic enhancers	HSMM	muscle
10	chr1:221883800-221890000	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr1:221884600-221891600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:221884800-221896200	Enhancers	Rectal Smooth Muscle	rectum
13	chr1:221885800-221892200	Enhancers	NHDF-Ad	bronchial
14	chr1:221886000-221895200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr1:221886200-221896000	Weak transcription	NHEK	skin
16	chr1:221886600-221889800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:221886600-221890600	Weak transcription	Adipose Nuclei	Adipose
18	chr1:221886600-221891600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr1:221886600-221891600	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr1:221886600-221891600	Weak transcription	Spleen	Spleen
21	chr1:221886600-221896000	Weak transcription	Aorta	Aorta
22	chr1:221886600-221897000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:221886600-221897000	Weak transcription	Duodenum Mucosa	Duodenum
24	chr1:221886600-221897000	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr1:221886800-221890000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr1:221886800-221890000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr1:221886800-221891000	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr1:221887200-221890000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr1:221887200-221890200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
30	chr1:221887200-221892200	Weak transcription	Thymus	Thymus
31	chr1:221887200-221899000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr1:221887400-221890400	Enhancers	Primary T cells fromperipheralblood	blood
33	chr1:221887400-221890600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr1:221887400-221893400	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr1:221887600-221890200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr1:221887600-221892000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr1:221887800-221890800	Enhancers	Fetal Intestine Small	intestine
38	chr1:221887800-221891400	Enhancers	Brain Angular Gyrus	brain
39	chr1:221887800-221892400	Weak transcription	Primary B cells from peripheral blood	blood
40	chr1:221887800-221893000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr1:221887800-221894000	Enhancers	Fetal Stomach	stomach
42	chr1:221887800-221898400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr1:221888000-221891000	Enhancers	Fetal Lung	lung
44	chr1:221888000-221891800	Enhancers	Stomach Smooth Muscle	stomach
45	chr1:221888000-221893200	Enhancers	Liver	Liver
46	chr1:221888000-221894400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr1:221888000-221899000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr1:221888000-221903000	Enhancers	Brain Hippocampus Middle	brain
49	chr1:221888200-221890000	Enhancers	K562	blood
50	chr1:221888200-221891600	Enhancers	A549	lung

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