Variant report

Variant	rs446202
Chromosome Location	chr4:106387755-106387756
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:106160813..106162575-chr4:106387724..106390093,2	K562	blood:
2	chr4:106366716..106368636-chr4:106386023..106388059,2	K562	blood:
3	chr4:106354166..106355972-chr4:106386471..106389222,2	K562	blood:
4	chr4:106385665..106390860-chr4:106392810..106395271,7	MCF-7	breast:
5	chr4:106372212..106374877-chr4:106385013..106387796,2	K562	blood:

Variant related genes	Relation type
ENSG00000138777	Chromatin interaction

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

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

rs_ID	r²[population]
rs369533	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879699	chr4:106212562-106698892	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv830027	chr4:106222010-106406738	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv1002228	chr4:106346206-106433381	ZNF genes & repeats Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:106327200-106389200	Weak transcription	Small Intestine	intestine
2	chr4:106327200-106390600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr4:106336800-106387800	Weak transcription	NHLF	lung
4	chr4:106340200-106387800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr4:106347600-106392800	Weak transcription	Colonic Mucosa	Colon
6	chr4:106348000-106388000	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr4:106348200-106387800	Weak transcription	Lung	lung
8	chr4:106348200-106393000	Weak transcription	Thymus	Thymus
9	chr4:106355400-106393200	Weak transcription	Esophagus	oesophagus
10	chr4:106357200-106392600	Weak transcription	Brain Angular Gyrus	brain
11	chr4:106357600-106392200	Weak transcription	Rectal Smooth Muscle	rectum
12	chr4:106361800-106387800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr4:106362200-106392600	Weak transcription	A549	lung
14	chr4:106363800-106390200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr4:106364600-106392000	Weak transcription	Brain Anterior Caudate	brain
16	chr4:106364600-106392600	Weak transcription	Fetal Kidney	kidney
17	chr4:106366000-106392400	Weak transcription	Osteobl	bone
18	chr4:106366000-106392600	Weak transcription	Psoas Muscle	Psoas
19	chr4:106366600-106392200	Weak transcription	Liver	Liver
20	chr4:106366600-106392200	Weak transcription	HepG2	liver
21	chr4:106366600-106392600	Weak transcription	Stomach Smooth Muscle	stomach
22	chr4:106366800-106393200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr4:106368200-106392000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr4:106369400-106388800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr4:106369600-106388000	Weak transcription	Hela-S3	cervix
26	chr4:106370000-106392600	Weak transcription	HUVEC	blood vessel
27	chr4:106373200-106392600	Weak transcription	NH-A	brain
28	chr4:106373400-106390600	Weak transcription	Colon Smooth Muscle	Colon
29	chr4:106373400-106392200	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr4:106374000-106387800	Weak transcription	Ovary	ovary
31	chr4:106374000-106392400	Weak transcription	NHDF-Ad	bronchial
32	chr4:106374000-106393000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr4:106374600-106392400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr4:106374600-106392600	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr4:106375000-106391400	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr4:106375400-106387800	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr4:106375400-106392600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr4:106375400-106393000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr4:106375400-106393000	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr4:106375600-106387800	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr4:106376800-106392600	Weak transcription	Fetal Lung	lung
42	chr4:106377000-106393000	Weak transcription	Right Atrium	heart
43	chr4:106377000-106393200	Weak transcription	Pancreas	Pancrea
44	chr4:106377000-106394000	Weak transcription	Gastric	stomach
45	chr4:106377600-106387800	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr4:106377800-106388600	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr4:106377800-106388800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr4:106378000-106387800	Weak transcription	Dnd41	blood
49	chr4:106378000-106387800	Weak transcription	NHEK	skin
50	chr4:106378000-106392200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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