Variant report

Variant	rs4731636
Chromosome Location	chr7:129536402-129536403
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:129531023..129532736-chr7:129534907..129537227,2	K562	blood:

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs16873739	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2280680	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3807118	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3807119	0.81[CEU][hapmap];0.82[CHB][hapmap];0.92[JPT][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3817530	0.87[CHB][hapmap]
rs4728179	0.90[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4731633	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4731634	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62491490	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62491495	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62491500	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62491519	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62491520	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62491531	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62491534	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62491535	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62491538	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62491540	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62491541	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533849	chr7:129462947-129616625	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv831129	chr7:129525406-129702477	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:129479400-129543600	Weak transcription	Thymus	Thymus
2	chr7:129497000-129536800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:129503400-129538400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:129505600-129545600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr7:129506000-129542800	Weak transcription	Small Intestine	intestine
6	chr7:129509600-129541000	Weak transcription	Spleen	Spleen
7	chr7:129510600-129541000	Weak transcription	Esophagus	oesophagus
8	chr7:129513200-129548600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr7:129516200-129542800	Weak transcription	HSMMtube	muscle
10	chr7:129516200-129584400	Weak transcription	Fetal Brain Male	brain
11	chr7:129517400-129543800	Weak transcription	Primary hematopoietic stem cells	blood
12	chr7:129518000-129537200	Weak transcription	Brain Angular Gyrus	brain
13	chr7:129518000-129537200	Weak transcription	Brain Cingulate Gyrus	brain
14	chr7:129518000-129545200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr7:129518200-129542600	Weak transcription	Fetal Muscle Trunk	muscle
16	chr7:129518200-129557200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:129518200-129564600	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr7:129518400-129538000	Weak transcription	Duodenum Mucosa	Duodenum
19	chr7:129519400-129546400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr7:129519600-129546400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr7:129520800-129541400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr7:129520800-129545600	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr7:129520800-129551200	Weak transcription	Placenta	Placenta
24	chr7:129521200-129537000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr7:129521200-129537800	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr7:129522000-129537200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr7:129522000-129541000	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr7:129522000-129548200	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr7:129522600-129541000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr7:129522600-129542600	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr7:129522600-129544600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr7:129522600-129547800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr7:129522600-129548400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr7:129522600-129548600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:129523200-129541000	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr7:129525400-129538200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr7:129525400-129541000	Weak transcription	Fetal Muscle Leg	muscle
38	chr7:129525400-129541000	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr7:129526000-129548200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr7:129526400-129538200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr7:129526400-129540800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr7:129526400-129540800	Weak transcription	NHLF	lung
43	chr7:129526600-129542600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr7:129527000-129538800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr7:129527000-129541000	Weak transcription	Liver	Liver
46	chr7:129527200-129541000	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr7:129527600-129538000	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr7:129527600-129541000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr7:129527800-129538800	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr7:129528400-129542200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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