Variant report

Variant	rs143950364
Chromosome Location	chr9:116126538-116126539
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:116037356..116039731-chr9:116125140..116127156,2	MCF-7	breast:
2	chr9:116125894..116128604-chr9:116186096..116187911,2	K562	blood:
3	chr9:116125080..116127101-chr9:116139095..116140609,2	K562	blood:
4	chr9:116125138..116127996-chr9:116129478..116132469,3	K562	blood:
5	chr9:116124299..116128919-chr9:116129296..116133206,5	K562	blood:
6	chr9:116118659..116121326-chr9:116124549..116126674,2	MCF-7	breast:
7	chr9:116108846..116117047-chr9:116126327..116140994,30	MCF-7	breast:
8	chr9:116116183..116118289-chr9:116124994..116127482,2	K562	blood:
9	chr9:116124595..116126724-chr9:116133634..116135834,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000119411	Chromatin interaction
ENSG00000119431	Chromatin interaction
ENSG00000176386	Chromatin interaction
ENSG00000136875	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

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	nsv530949	chr9:115821128-116487796	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv1042663	chr9:115920158-116167140	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv893744	chr9:115934852-116170227	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	nsv519849	chr9:116111407-116144973	Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1036586	chr9:116118902-116136993	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
6	nsv615214	chr9:116125789-116149967	Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116113000-116135600	Weak transcription	Colonic Mucosa	Colon
2	chr9:116113000-116138000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr9:116113400-116135200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr9:116113800-116137800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr9:116114000-116127400	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr9:116114200-116136400	Weak transcription	Primary B cells from cord blood	blood
7	chr9:116115400-116135000	Weak transcription	Esophagus	oesophagus
8	chr9:116115600-116132800	Weak transcription	Fetal Intestine Large	intestine
9	chr9:116116400-116137000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr9:116120200-116131800	Weak transcription	Lung	lung
11	chr9:116120400-116127200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr9:116123000-116132800	Weak transcription	Fetal Stomach	stomach
13	chr9:116123200-116129200	Enhancers	Hela-S3	cervix
14	chr9:116123200-116131800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:116123200-116136400	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr9:116123600-116138200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr9:116123800-116130400	Weak transcription	Stomach Mucosa	stomach
18	chr9:116124000-116135000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr9:116124000-116135000	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr9:116124000-116135600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr9:116124000-116135600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr9:116124200-116127800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr9:116124400-116128400	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr9:116124400-116131600	Weak transcription	Pancreas	Pancrea
25	chr9:116124400-116135600	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr9:116124800-116128800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr9:116124800-116134200	Weak transcription	Brain Anterior Caudate	brain
28	chr9:116124800-116134400	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr9:116124800-116135000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr9:116124800-116135200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr9:116124800-116135400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr9:116124800-116135800	Weak transcription	Brain Substantia Nigra	brain
33	chr9:116125000-116130600	Weak transcription	Gastric	stomach
34	chr9:116125000-116138000	Weak transcription	Fetal Kidney	kidney
35	chr9:116125200-116133600	Weak transcription	Duodenum Mucosa	Duodenum
36	chr9:116125200-116135000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr9:116125800-116126800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr9:116125800-116128200	Enhancers	K562	blood
39	chr9:116126200-116134400	Weak transcription	Placenta	Placenta
40	chr9:116126400-116127400	Weak transcription	Primary hematopoietic stem cells	blood
41	chr9:116126400-116128200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr9:116126400-116128600	Weak transcription	Fetal Intestine Small	intestine

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