Variant report

Variant	rs34704879
Chromosome Location	chr9:71873285-71873286
allele	A/C
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	POLR2A	chr9:71872657-71873306	HepG2	liver:	n/a	n/a

Variant related genes	Relation type
ENSG00000269295	TF binding region

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs13288610	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051723	chr9:71398713-71971285	Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv931684	chr9:71417110-71957723	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh 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	31 gene(s)	inside rSNPs	diseases
3	nsv1049175	chr9:71418242-71986910	Weak transcription Active TSS Enhancers Strong transcription Flanking 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	31 gene(s)	inside rSNPs	diseases
4	nsv1035823	chr9:71465139-71901672	Genic enhancers Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv466396	chr9:71471912-71935577	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	nsv614548	chr9:71471912-71935577	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats 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	25 gene(s)	inside rSNPs	diseases
7	nsv1035477	chr9:71511927-71959487	Enhancers Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
8	nsv893416	chr9:71597840-71888601	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
9	nsv817406	chr9:71675454-72179318	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer 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	25 gene(s)	inside rSNPs	diseases
10	nsv831610	chr9:71846941-72016835	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
11	esv1796249	chr9:71862129-71911566	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71828800-71874200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr9:71836400-71874000	Weak transcription	Fetal Brain Male	brain
3	chr9:71847600-71879600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr9:71852000-71876800	Weak transcription	Psoas Muscle	Psoas
5	chr9:71863800-71874200	Weak transcription	Rectal Smooth Muscle	rectum
6	chr9:71864600-71876800	Weak transcription	Fetal Heart	heart
7	chr9:71864600-71880800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr9:71864800-71880800	Weak transcription	NHDF-Ad	bronchial
9	chr9:71866400-71881000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr9:71866600-71873800	Weak transcription	HSMM	muscle
11	chr9:71868400-71874800	Weak transcription	Fetal Muscle Leg	muscle
12	chr9:71868800-71875000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr9:71869000-71875000	Weak transcription	Brain Angular Gyrus	brain
14	chr9:71869000-71879400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr9:71869400-71873400	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr9:71869400-71873400	Weak transcription	Small Intestine	intestine
17	chr9:71869400-71873600	Weak transcription	Colonic Mucosa	Colon
18	chr9:71869400-71873800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr9:71869400-71875200	Weak transcription	Aorta	Aorta
20	chr9:71869400-71876600	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr9:71869400-71879600	Weak transcription	Right Ventricle	heart
22	chr9:71869400-71887200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr9:71869600-71874400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr9:71869600-71874400	Weak transcription	NHEK	skin
25	chr9:71869600-71874600	Weak transcription	Primary T cells from cord blood	blood
26	chr9:71869600-71879400	Weak transcription	Left Ventricle	heart
27	chr9:71869600-71879600	Weak transcription	Pancreas	Pancrea
28	chr9:71869600-71881000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr9:71869600-71881000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr9:71869800-71881000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr9:71869800-71883000	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr9:71870000-71873400	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr9:71870000-71873600	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr9:71870000-71876600	Weak transcription	HepG2	liver
35	chr9:71870000-71879600	Weak transcription	Osteobl	bone
36	chr9:71870200-71874000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr9:71870200-71874000	Weak transcription	GM12878-XiMat	blood
38	chr9:71870400-71880200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr9:71870600-71878400	Weak transcription	Fetal Lung	lung
40	chr9:71871800-71874000	Weak transcription	Esophagus	oesophagus
41	chr9:71871800-71879400	Weak transcription	Gastric	stomach
42	chr9:71871800-71880600	Weak transcription	Stomach Mucosa	stomach
43	chr9:71871800-71881000	Weak transcription	HUVEC	blood vessel
44	chr9:71872000-71873600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr9:71872000-71875400	Weak transcription	Fetal Intestine Small	intestine
46	chr9:71872000-71880800	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr9:71872000-71880800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr9:71872200-71873800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr9:71872200-71873800	Weak transcription	Placenta	Placenta
50	chr9:71872200-71874400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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