Variant report

Variant	rs73110844
Chromosome Location	chr1:221893646-221893647
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:221891993..221895094-chr1:221895705..221898533,3	K562	blood:
2	chr1:221883604..221886254-chr1:221893154..221895130,3	K562	blood:
3	chr1:221887650..221891571-chr1:221892438..221898117,9	K562	blood:

Variant related genes	Relation type
ENSG00000143507	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs12057339	1.00[AMR][1000 genomes]
rs12059970	1.00[AMR][1000 genomes]
rs12068699	1.00[AMR][1000 genomes]
rs12069068	1.00[AMR][1000 genomes]
rs12074253	1.00[AMR][1000 genomes]
rs12095091	1.00[AMR][1000 genomes]
rs12095764	1.00[AMR][1000 genomes]
rs55927813	1.00[AMR][1000 genomes]
rs55952360	1.00[AMR][1000 genomes]
rs56906577	1.00[AMR][1000 genomes]
rs74145398	1.00[AMR][1000 genomes]
rs74147814	1.00[AMR][1000 genomes]
rs74147822	1.00[AMR][1000 genomes]
rs74147825	1.00[AMR][1000 genomes]
rs74147826	1.00[AMR][1000 genomes]
rs74147828	1.00[AMR][1000 genomes]
rs74147829	1.00[AMR][1000 genomes]
rs74147830	1.00[AMR][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:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221879600-221902400	Enhancers	Brain Substantia Nigra	brain
2	chr1:221879800-221896800	Enhancers	Colon Smooth Muscle	Colon
3	chr1:221882800-221899000	Genic enhancers	HSMM	muscle
4	chr1:221884800-221896200	Enhancers	Rectal Smooth Muscle	rectum
5	chr1:221886000-221895200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr1:221886200-221896000	Weak transcription	NHEK	skin
7	chr1:221886600-221896000	Weak transcription	Aorta	Aorta
8	chr1:221886600-221897000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:221886600-221897000	Weak transcription	Duodenum Mucosa	Duodenum
10	chr1:221886600-221897000	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr1:221887200-221899000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr1:221887800-221894000	Enhancers	Fetal Stomach	stomach
13	chr1:221887800-221898400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr1:221888000-221894400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr1:221888000-221899000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr1:221888000-221903000	Enhancers	Brain Hippocampus Middle	brain
17	chr1:221888600-221894000	Enhancers	NHLF	lung
18	chr1:221888600-221896800	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr1:221888800-221898600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr1:221889000-221896600	Weak transcription	Primary T cells from cord blood	blood
21	chr1:221889400-221899600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr1:221889600-221896400	Weak transcription	Dnd41	blood
23	chr1:221889800-221899000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr1:221890400-221895400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr1:221890400-221898400	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr1:221890600-221894800	Strong transcription	GM12878-XiMat	blood
27	chr1:221890600-221895600	Weak transcription	Fetal Muscle Trunk	muscle
28	chr1:221890600-221896400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:221890600-221896600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr1:221890800-221896200	Weak transcription	Fetal Intestine Small	intestine
31	chr1:221890800-221906400	Weak transcription	Right Ventricle	heart
32	chr1:221890800-221910200	Weak transcription	Lung	lung
33	chr1:221891200-221893800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr1:221891600-221894400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:221891800-221894800	Weak transcription	Fetal Thymus	thymus
36	chr1:221891800-221911000	Weak transcription	Gastric	stomach
37	chr1:221891800-221913000	Weak transcription	Fetal Intestine Large	intestine
38	chr1:221892200-221895200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr1:221892200-221898200	Enhancers	HSMMtube	muscle
40	chr1:221892400-221894000	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr1:221892400-221894200	Enhancers	NH-A	brain
42	chr1:221892400-221896600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr1:221892400-221901400	Weak transcription	Small Intestine	intestine
44	chr1:221892600-221894200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr1:221892600-221894200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr1:221892600-221896200	Enhancers	Osteobl	bone
47	chr1:221892600-221898000	Weak transcription	Stomach Mucosa	stomach
48	chr1:221892800-221894000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr1:221892800-221894800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr1:221892800-221894800	Genic enhancers	Muscle Satellite Cultured Cells	--

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