Variant report

Variant	rs567156558
Chromosome Location	chr10:49616686-49616687
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:49615597..49618030-chr10:49714235..49716218,3	K562	blood:
2	chr10:49615995..49618408-chr10:49619011..49621814,2	K562	blood:
3	chr10:49613380..49617347-chr10:49637674..49642930,5	K562	blood:

Variant related genes	Relation type
ENSG00000107643	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv895372	chr10:49576878-49933488	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1039508	chr10:49595718-49654403	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv825373	chr10:49616204-49617680	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49598600-49619800	Weak transcription	Fetal Intestine Small	intestine
2	chr10:49599200-49622200	Weak transcription	HepG2	liver
3	chr10:49599800-49618000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr10:49600000-49618600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr10:49600200-49617400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr10:49600200-49618200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr10:49600400-49616800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr10:49600400-49620200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr10:49605200-49618000	Weak transcription	Fetal Muscle Leg	muscle
10	chr10:49606800-49619800	Weak transcription	Fetal Stomach	stomach
11	chr10:49607600-49616800	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr10:49607600-49618000	Weak transcription	Fetal Muscle Trunk	muscle
13	chr10:49607600-49619400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr10:49607600-49619600	Weak transcription	Colonic Mucosa	Colon
15	chr10:49607600-49619600	Weak transcription	Rectal Smooth Muscle	rectum
16	chr10:49607600-49624200	Weak transcription	Gastric	stomach
17	chr10:49607600-49624200	Weak transcription	Lung	lung
18	chr10:49607600-49647800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr10:49607600-49652400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr10:49607800-49616800	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr10:49607800-49620400	Weak transcription	Stomach Mucosa	stomach
22	chr10:49608000-49645600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr10:49608200-49618000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr10:49608200-49618200	Weak transcription	Fetal Kidney	kidney
25	chr10:49608200-49619400	Weak transcription	Colon Smooth Muscle	Colon
26	chr10:49608200-49621000	Weak transcription	Small Intestine	intestine
27	chr10:49608200-49634400	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr10:49608400-49618200	Weak transcription	Duodenum Mucosa	Duodenum
29	chr10:49608600-49620200	Weak transcription	Right Ventricle	heart
30	chr10:49608800-49616800	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr10:49608800-49618000	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr10:49608800-49618200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr10:49608800-49618600	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr10:49609000-49617800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr10:49609000-49620000	Weak transcription	Brain Hippocampus Middle	brain
36	chr10:49609000-49620600	Weak transcription	Hela-S3	cervix
37	chr10:49609200-49616800	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr10:49609200-49618000	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr10:49609200-49618000	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr10:49609200-49618000	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr10:49609200-49618000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr10:49609200-49618000	Weak transcription	Brain Anterior Caudate	brain
43	chr10:49609200-49618000	Weak transcription	Brain Cingulate Gyrus	brain
44	chr10:49609200-49618000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr10:49609200-49618200	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr10:49609200-49620000	Weak transcription	GM12878-XiMat	blood
47	chr10:49609200-49620800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr10:49609400-49618200	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr10:49609400-49618800	Weak transcription	Fetal Brain Male	brain
50	chr10:49609600-49618000	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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