Variant report

Variant	rs73857903
Chromosome Location	chr3:121236666-121236667
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:121228286..121231093-chr3:121234825..121237774,2	K562	blood:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs3218652	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58297766	1.00[AMR][1000 genomes]
rs58466835	1.00[AMR][1000 genomes]
rs58525071	1.00[AMR][1000 genomes]
rs58881799	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58922309	1.00[AMR][1000 genomes]
rs60108064	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60204652	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61004683	1.00[AMR][1000 genomes]
rs61040872	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72971952	1.00[AMR][1000 genomes]
rs72971955	1.00[AMR][1000 genomes]
rs73855375	1.00[AMR][1000 genomes]
rs73855376	1.00[AMR][1000 genomes]
rs73855378	1.00[AMR][1000 genomes]
rs73855380	1.00[AMR][1000 genomes]
rs73855381	1.00[AMR][1000 genomes]
rs73855385	1.00[AMR][1000 genomes]
rs73855388	1.00[AMR][1000 genomes]
rs73855389	1.00[AMR][1000 genomes]
rs73855390	1.00[AMR][1000 genomes]
rs73855391	1.00[AMR][1000 genomes]
rs73855392	1.00[AMR][1000 genomes]
rs73855394	1.00[AMR][1000 genomes]
rs73855395	1.00[AMR][1000 genomes]
rs73855396	1.00[AMR][1000 genomes]
rs73855397	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73855399	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73855400	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73855402	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73857906	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73857907	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73857909	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73857910	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998555	chr3:120700604-121348015	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
2	nsv591395	chr3:120970900-121501070	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv591396	chr3:120970900-121557533	Strong transcription Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv591397	chr3:120977383-121505882	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
5	nsv591400	chr3:121070299-121339354	Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv999335	chr3:121100283-121408766	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv877381	chr3:121192350-121343500	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv1007522	chr3:121200563-121374051	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121151200-121263800	Weak transcription	Duodenum Mucosa	Duodenum
2	chr3:121177200-121237000	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr3:121178200-121263800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr3:121186400-121255600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr3:121193200-121237000	Weak transcription	Fetal Muscle Trunk	muscle
6	chr3:121200600-121264000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr3:121201000-121250600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr3:121202400-121263200	Weak transcription	NHLF	lung
9	chr3:121202400-121263800	Weak transcription	HSMM	muscle
10	chr3:121209400-121263600	Weak transcription	NHDF-Ad	bronchial
11	chr3:121210000-121246400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr3:121210200-121241400	Weak transcription	Fetal Muscle Leg	muscle
13	chr3:121229000-121238600	Weak transcription	HMEC	breast
14	chr3:121229000-121239200	Weak transcription	HUVEC	blood vessel
15	chr3:121229000-121244600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr3:121229000-121253200	Weak transcription	HepG2	liver
17	chr3:121229600-121263000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr3:121230600-121239400	Weak transcription	Fetal Stomach	stomach
19	chr3:121230800-121260200	Strong transcription	Dnd41	blood
20	chr3:121232200-121263800	Weak transcription	Fetal Heart	heart
21	chr3:121233200-121242400	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr3:121233400-121241000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr3:121233400-121242200	Strong transcription	A549	lung
24	chr3:121233400-121263000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr3:121233600-121237200	Strong transcription	Primary neutrophils fromperipheralblood	blood
26	chr3:121233600-121241800	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr3:121233600-121245600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr3:121233800-121237000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr3:121233800-121237200	ZNF genes & repeats	GM12878-XiMat	blood
30	chr3:121233800-121248800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr3:121234000-121264000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr3:121234200-121238600	Weak transcription	NHEK	skin
33	chr3:121234200-121263600	Weak transcription	Osteobl	bone
34	chr3:121234200-121264000	Weak transcription	Fetal Intestine Large	intestine
35	chr3:121234400-121245000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr3:121234400-121263200	Strong transcription	HUES64 Cell Line	embryonic stem cell
37	chr3:121234600-121236800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
38	chr3:121234600-121237400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr3:121234600-121238600	Weak transcription	Thymus	Thymus
40	chr3:121234600-121245800	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr3:121234600-121263600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr3:121234800-121237000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr3:121235000-121242200	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr3:121235000-121263800	Weak transcription	Primary B cells from cord blood	blood
45	chr3:121235000-121264000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr3:121235400-121236800	Strong transcription	Hela-S3	cervix
47	chr3:121235400-121237400	Weak transcription	Primary T cells from cord blood	blood
48	chr3:121235400-121244800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr3:121235400-121263600	Weak transcription	Brain Germinal Matrix	brain
50	chr3:121235600-121242200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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