Variant report

Variant	rs10992629
Chromosome Location	chr9:95854444-95854445
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	FOSL2	chr9:95853534-95854457	A549	lung:	n/a	chr9:95854250-95854258 chr9:95853926-95853937
2	JUND	chr9:95853574-95854471	SK-N-SH	brain:	n/a	chr9:95853925-95853936 chr9:95854250-95854258 chr9:95853907-95853918
3	FOSL2	chr9:95853596-95854452	SK-N-SH	brain:	n/a	chr9:95854250-95854258 chr9:95853926-95853937
4	FOSL2	chr9:95853631-95854523	MCF-7	breast:	n/a	chr9:95854250-95854258 chr9:95853926-95853937
5	JUND	chr9:95853542-95854530	HCT-116	colon:	n/a	chr9:95853925-95853936 chr9:95854250-95854258 chr9:95853907-95853918
6	MAX	chr9:95853619-95854507	A549	lung:	n/a	chr9:95854250-95854259
7	MTA3	chr9:95853519-95854526	GM12878	blood:	n/a	n/a
8	FOSL1	chr9:95853444-95854507	HCT-116	colon:	n/a	chr9:95854250-95854258 chr9:95853907-95853918 chr9:95853925-95853936
9	CBX3	chr9:95853388-95854513	HCT-116	colon:	n/a	n/a
10	SP1	chr9:95853529-95854528	HCT-116	colon:	n/a	n/a
11	FOXA2	chr9:95853995-95854509	A549	lung:	n/a	n/a
12	TCF12	chr9:95853495-95854537	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:95853194..95855867-chr9:95863177..95866078,2	MCF-7	breast:
2	chr9:95828110..95830344-chr9:95853577..95856125,2	K562	blood:
3	chr9:95816364..95826268-chr9:95852309..95863275,20	MCF-7	breast:
4	chr9:95838033..95840952-chr9:95852515..95855159,2	MCF-7	breast:
5	chr9:95839549..95841573-chr9:95854278..95856660,2	MCF-7	breast:
6	chr9:95852876..95854793-chr9:95906541..95909391,2	K562	blood:
7	chr9:95797817..95800116-chr9:95854194..95855844,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NINJ1-1	chr9:95854274-95855174	NONHSAT133230

Variant related genes	Relation type
C9orf89	TF binding region
ENSG00000203364	Chromatin interaction
ENSG00000157303	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs10761192	0.82[CHD][hapmap]
rs7028691	0.91[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526296	chr9:95708192-96030392	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv1054767	chr9:95738134-95875977	Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1035230	chr9:95770249-95934982	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv893576	chr9:95789960-96158277	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	esv1824329	chr9:95811604-95921347	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers 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	23 gene(s)	inside rSNPs	diseases
6	nsv893577	chr9:95812707-95872216	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv893578	chr9:95818641-95887320	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats 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	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95834400-95857400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:95836200-95855600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr9:95840400-95857000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:95845200-95857200	Weak transcription	Small Intestine	intestine
5	chr9:95845800-95854800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr9:95846200-95855000	Weak transcription	Fetal Lung	lung
7	chr9:95846400-95857000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr9:95848400-95854600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr9:95848400-95854800	Weak transcription	Fetal Intestine Large	intestine
10	chr9:95848400-95855000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr9:95848400-95855000	Weak transcription	Duodenum Mucosa	Duodenum
12	chr9:95848400-95855400	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr9:95848400-95855800	Weak transcription	Liver	Liver
14	chr9:95848600-95855000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr9:95848600-95857000	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr9:95848800-95855400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr9:95848800-95855600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr9:95849400-95855200	Weak transcription	Fetal Kidney	kidney
19	chr9:95849400-95857400	Weak transcription	Ovary	ovary
20	chr9:95849600-95855000	Weak transcription	Colonic Mucosa	Colon
21	chr9:95849600-95855200	Weak transcription	Fetal Intestine Small	intestine
22	chr9:95850400-95855400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr9:95851000-95855000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr9:95851400-95855200	Weak transcription	Thymus	Thymus
25	chr9:95851600-95854800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr9:95851800-95855400	Weak transcription	K562	blood
27	chr9:95852000-95855000	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr9:95852200-95855400	Weak transcription	Primary T cells from cord blood	blood
29	chr9:95852600-95856800	Enhancers	Primary B cells from peripheral blood	blood
30	chr9:95853200-95854800	ZNF genes & repeats	GM12878-XiMat	blood
31	chr9:95853400-95854800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr9:95853400-95857000	Enhancers	Primary B cells from cord blood	blood
33	chr9:95853400-95857200	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr9:95853400-95857200	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr9:95853600-95855200	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr9:95853600-95856800	Enhancers	HepG2	liver
37	chr9:95853600-95857200	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr9:95853800-95855000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr9:95853800-95857200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr9:95854000-95854600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr9:95854000-95854600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr9:95854000-95854600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr9:95854000-95854800	Enhancers	HMEC	breast
44	chr9:95854000-95854800	Enhancers	NH-A	brain
45	chr9:95854000-95855000	Enhancers	Osteobl	bone
46	chr9:95854000-95855200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr9:95854000-95855200	Enhancers	NHLF	lung
48	chr9:95854000-95855400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr9:95854000-95856000	Enhancers	Hela-S3	cervix
50	chr9:95854000-95856200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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