Variant report

Variant	rs111592449
Chromosome Location	chr9:100942666-100942667
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:100879718..100885853-chr9:100942357..100948328,6	K562	blood:
2	chr9:100817456..100819195-chr9:100941306..100944143,2	K562	blood:
3	chr9:100930925..100932866-chr9:100942560..100944463,2	K562	blood:
4	chr9:100881221..100884205-chr9:100940045..100942991,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000106785	Chromatin interaction
ENSG00000095380	Chromatin interaction

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

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	nsv482635	chr9:100775549-100953239	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv893613	chr9:100885779-100943397	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv1053729	chr9:100909554-100997718	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv520067	chr9:100927161-100978542	Genic enhancers Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv430085	chr9:100928245-101339645	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv831663	chr9:100941048-101109492	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
7	esv3358729	chr9:100942546-100944216	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:100931800-100954400	Weak transcription	Right Atrium	heart
2	chr9:100932800-100951200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr9:100933400-100951400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr9:100933800-100950200	Weak transcription	Colonic Mucosa	Colon
5	chr9:100933800-100951400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr9:100934400-100954000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr9:100935200-100947800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr9:100935400-100953000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr9:100935400-100953000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr9:100935400-100953200	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr9:100935800-100944800	Weak transcription	Lung	lung
12	chr9:100936000-100953000	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr9:100936000-100953200	Weak transcription	Gastric	stomach
14	chr9:100937000-100948400	Weak transcription	Small Intestine	intestine
15	chr9:100937400-100947000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr9:100937800-100947400	Weak transcription	NHEK	skin
17	chr9:100937800-100951400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr9:100937800-100953200	Weak transcription	Primary hematopoietic stem cells	blood
19	chr9:100938000-100943800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr9:100938000-100943800	Weak transcription	Spleen	Spleen
21	chr9:100938000-100945400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr9:100938000-100949800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr9:100938000-100952600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr9:100938000-100953000	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr9:100939400-100947400	Weak transcription	Thymus	Thymus
26	chr9:100939600-100944600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr9:100939600-100945800	Enhancers	Duodenum Mucosa	Duodenum
28	chr9:100939800-100944200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr9:100939800-100944400	Weak transcription	Stomach Mucosa	stomach
30	chr9:100939800-100944600	Weak transcription	Liver	Liver
31	chr9:100940000-100951400	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr9:100940400-100952400	Genic enhancers	Fetal Intestine Small	intestine
33	chr9:100940600-100947200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr9:100941000-100942800	Enhancers	Fetal Thymus	thymus
35	chr9:100941400-100943400	Enhancers	Primary T cells fromperipheralblood	blood
36	chr9:100941400-100943400	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr9:100941600-100942800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr9:100941600-100944800	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr9:100941600-100945800	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr9:100941800-100943000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr9:100941800-100943000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr9:100941800-100943000	Enhancers	K562	blood
43	chr9:100941800-100946400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr9:100941800-100947800	Weak transcription	Esophagus	oesophagus
45	chr9:100941800-100949800	Enhancers	Fetal Intestine Large	intestine
46	chr9:100941800-100954000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr9:100942000-100946800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr9:100942200-100942800	Enhancers	Primary T cells from cord blood	blood
49	chr9:100942400-100942800	Enhancers	Primary B cells from cord blood	blood
50	chr9:100942400-100943000	Enhancers	ES-I3 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links