Variant report

Variant	rs10779730
Chromosome Location	chr1:9798894-9798895
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:9790884..9795814-chr1:9797225..9799238,5	K562	blood:
2	chr1:9795106..9799024-chr1:9799834..9803861,3	K562	blood:

Variant related genes	Relation type
ENSG00000171603	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10779731	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10864437	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10864438	0.94[ASN][1000 genomes]
rs11121484	0.87[AMR][1000 genomes]
rs11121485	0.85[EUR][1000 genomes]
rs11121486	0.85[EUR][1000 genomes]
rs11121488	0.85[EUR][1000 genomes]
rs11121489	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11121490	0.93[ASN][1000 genomes]
rs1141402	0.80[EUR][1000 genomes]
rs11674	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11804356	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11806520	0.88[ASN][1000 genomes]
rs12021914	0.91[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12025864	0.80[EUR][1000 genomes]
rs12034313	0.80[EUR][1000 genomes]
rs12037599	0.80[EUR][1000 genomes]
rs12042293	0.85[EUR][1000 genomes]
rs12047054	0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12064975	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12088273	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1220419	0.80[ASN][1000 genomes]
rs12568720	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12569008	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1615629	0.88[ASN][1000 genomes]
rs1660741	0.88[ASN][1000 genomes]
rs1660742	0.88[ASN][1000 genomes]
rs4512653	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4845975	0.84[ASN][1000 genomes]
rs56109009	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72855716	0.94[ASN][1000 genomes]
rs7526958	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7550246	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7550295	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3385337	chr1:9105242-10082223	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	549 gene(s)	inside rSNPs	diseases
2	nsv871610	chr1:9655795-10008221	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	esv3417409	chr1:9683992-10241703	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	nsv832203	chr1:9726632-9860209	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:9750600-9813000	Weak transcription	Right Atrium	heart
2	chr1:9781200-9813200	Strong transcription	Stomach Smooth Muscle	stomach
3	chr1:9781600-9800600	Weak transcription	Fetal Brain Male	brain
4	chr1:9783800-9799600	Strong transcription	Fetal Brain Female	brain
5	chr1:9784000-9815400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:9784200-9807400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr1:9784200-9815800	Strong transcription	Fetal Intestine Small	intestine
8	chr1:9786400-9814000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr1:9786600-9802200	Strong transcription	Esophagus	oesophagus
10	chr1:9786600-9804800	Strong transcription	Ovary	ovary
11	chr1:9786600-9806000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr1:9786600-9807000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr1:9786600-9807000	Strong transcription	HepG2	liver
14	chr1:9786600-9815200	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr1:9786800-9802600	Strong transcription	Osteobl	bone
16	chr1:9786800-9806200	Strong transcription	Rectal Mucosa Donor 31	rectum
17	chr1:9786800-9807200	Strong transcription	Placenta	Placenta
18	chr1:9786800-9814000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr1:9787000-9801600	Strong transcription	Gastric	stomach
20	chr1:9787000-9801600	Strong transcription	Right Ventricle	heart
21	chr1:9787000-9805600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:9787000-9807000	Strong transcription	H1 Cell Line	embryonic stem cell
23	chr1:9787000-9813000	Weak transcription	Fetal Heart	heart
24	chr1:9787200-9802400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
25	chr1:9787200-9804800	Strong transcription	HUES48 Cell Line	embryonic stem cell
26	chr1:9787200-9806800	Strong transcription	Duodenum Smooth Muscle	Duodenum
27	chr1:9787200-9807200	Strong transcription	Fetal Muscle Leg	muscle
28	chr1:9787400-9801800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr1:9787400-9806400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
30	chr1:9787400-9807000	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr1:9787400-9807200	Strong transcription	Left Ventricle	heart
32	chr1:9787400-9807200	Strong transcription	Sigmoid Colon	Sigmoid Colon
33	chr1:9787400-9811800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr1:9787600-9802200	Strong transcription	Skeletal Muscle Male	skeletal muscle
35	chr1:9787600-9807400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr1:9787600-9812000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr1:9787600-9813200	Strong transcription	Fetal Muscle Trunk	muscle
38	chr1:9787600-9815200	Strong transcription	Duodenum Mucosa	Duodenum
39	chr1:9788000-9802400	Strong transcription	Brain Hippocampus Middle	brain
40	chr1:9788000-9807000	Strong transcription	NHEK	skin
41	chr1:9788200-9799600	Strong transcription	Pancreas	Pancrea
42	chr1:9788200-9804800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:9788400-9807400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr1:9788400-9811800	Strong transcription	Cortex derived primary cultured neurospheres	brain
45	chr1:9788600-9799600	Strong transcription	Skeletal Muscle Female	skeletal muscle
46	chr1:9788600-9801800	Strong transcription	Brain Substantia Nigra	brain
47	chr1:9789200-9799600	Strong transcription	Fetal Lung	lung
48	chr1:9789400-9802400	Strong transcription	Colon Smooth Muscle	Colon
49	chr1:9789800-9815400	Strong transcription	Fetal Thymus	thymus
50	chr1:9789800-9815800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood

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