Variant report

Variant	rs16844028
Chromosome Location	chr4:3195250-3195251
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:3169372..3171758-chr4:3194914..3197788,2	K562	blood:
2	chr4:3110448..3112382-chr4:3193670..3195664,2	MCF-7	breast:
3	chr4:3187730..3190882-chr4:3194133..3197164,3	K562	blood:

Extended variants
information (count: 103 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs10006373	0.93[EUR][1000 genomes]
rs10012793	0.81[EUR][1000 genomes]
rs10021254	1.00[CEU][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10034669	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10155264	1.00[CEU][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10488840	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1065745	1.00[ASN][1000 genomes]
rs16843803	1.00[ASN][1000 genomes]
rs16844026	1.00[CEU][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17780617	1.00[ASN][1000 genomes]
rs2003530	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2005787	0.95[EUR][1000 genomes]
rs28436280	0.90[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28507598	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28643391	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3025825	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34045730	1.00[ASN][1000 genomes]
rs34591077	1.00[ASN][1000 genomes]
rs362269	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs362274	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs362276	0.88[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs362278	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs362303	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs362304	1.00[ASN][1000 genomes]
rs362305	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs362310	1.00[CEU][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs362323	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs362325	0.84[CEU][hapmap];0.93[YRI][hapmap];0.85[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs362338	1.00[CEU][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs363065	1.00[ASN][1000 genomes]
rs363069	1.00[ASN][1000 genomes]
rs363071	1.00[ASN][1000 genomes]
rs363078	1.00[ASN][1000 genomes]
rs363084	1.00[ASN][1000 genomes]
rs363087	1.00[ASN][1000 genomes]
rs363089	1.00[ASN][1000 genomes]
rs363090	0.93[EUR][1000 genomes]
rs363091	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs363093	0.93[EUR][1000 genomes]
rs363094	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs363095	1.00[CEU][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs363097	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs363098	1.00[EUR][1000 genomes]
rs363100	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs363101	0.95[EUR][1000 genomes]
rs363103	1.00[ASN][1000 genomes]
rs363105	1.00[ASN][1000 genomes]
rs363106	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs363124	0.93[EUR][1000 genomes]
rs363125	0.93[EUR][1000 genomes]
rs363128	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs363141	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs56794194	1.00[ASN][1000 genomes]
rs57196404	1.00[ASN][1000 genomes]
rs59588638	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61460614	1.00[ASN][1000 genomes]
rs61583241	1.00[ASN][1000 genomes]
rs61790489	1.00[ASN][1000 genomes]
rs61790490	1.00[ASN][1000 genomes]
rs61792472	1.00[ASN][1000 genomes]
rs61792477	1.00[ASN][1000 genomes]
rs61792500	1.00[ASN][1000 genomes]
rs61792501	1.00[ASN][1000 genomes]
rs61792502	1.00[ASN][1000 genomes]
rs61792503	1.00[ASN][1000 genomes]
rs61792505	1.00[ASN][1000 genomes]
rs61792507	1.00[ASN][1000 genomes]
rs61792508	1.00[ASN][1000 genomes]
rs61792509	1.00[ASN][1000 genomes]
rs61792510	1.00[ASN][1000 genomes]
rs61792512	1.00[ASN][1000 genomes]
rs61792515	1.00[ASN][1000 genomes]
rs61792531	1.00[ASN][1000 genomes]
rs61792532	1.00[ASN][1000 genomes]
rs61792533	1.00[ASN][1000 genomes]
rs61792535	0.87[EUR][1000 genomes]
rs6446724	1.00[EUR][1000 genomes]
rs6446725	1.00[EUR][1000 genomes]
rs6828615	0.88[EUR][1000 genomes]
rs6828882	0.99[EUR][1000 genomes]
rs6834455	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs6835567	0.92[EUR][1000 genomes]
rs6839081	0.93[EUR][1000 genomes]
rs6839274	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs6843895	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs73073018	1.00[ASN][1000 genomes]
rs7438553	0.96[EUR][1000 genomes]
rs7654034	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs7665816	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs7667354	1.00[EUR][1000 genomes]
rs7674122	1.00[ASN][1000 genomes]
rs7683309	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7686771	1.00[ASN][1000 genomes]
rs7688390	0.85[EUR][1000 genomes]
rs7699037	1.00[ASN][1000 genomes]
rs9993781	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3418626	chr4:2741174-3461492	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	esv3397632	chr4:2741239-3460583	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
3	nsv461163	chr4:2906285-3234980	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
4	nsv593437	chr4:2906285-3234980	Genic enhancers Active TSS Strong transcription Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
5	nsv461164	chr4:3149016-3215835	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
6	nsv593439	chr4:3149016-3215835	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
7	nsv998290	chr4:3176454-3355758	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3114600-3292400	Weak transcription	Right Atrium	heart
2	chr4:3145800-3239200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr4:3167800-3203400	Strong transcription	Primary B cells from peripheral blood	blood
4	chr4:3168000-3197600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr4:3168000-3202800	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr4:3168000-3203000	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr4:3170000-3208800	Weak transcription	Stomach Mucosa	stomach
8	chr4:3171200-3197600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr4:3172000-3202800	Strong transcription	Duodenum Mucosa	Duodenum
10	chr4:3172200-3195400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr4:3172400-3199800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr4:3172400-3238800	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr4:3172800-3202800	Strong transcription	Rectal Mucosa Donor 29	rectum
14	chr4:3173600-3200000	Strong transcription	HUES48 Cell Line	embryonic stem cell
15	chr4:3174000-3204000	Strong transcription	Stomach Smooth Muscle	stomach
16	chr4:3176400-3199600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:3178800-3200000	Strong transcription	Skeletal Muscle Male	skeletal muscle
18	chr4:3181000-3201400	Weak transcription	Hela-S3	cervix
19	chr4:3181600-3206600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr4:3182400-3203200	Strong transcription	Fetal Intestine Large	intestine
21	chr4:3183000-3197400	Strong transcription	Dnd41	blood
22	chr4:3183000-3202600	Strong transcription	Liver	Liver
23	chr4:3183400-3206800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr4:3185200-3208400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr4:3186000-3195600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr4:3189200-3199800	Strong transcription	Primary B cells from cord blood	blood
27	chr4:3190600-3203600	Weak transcription	Small Intestine	intestine
28	chr4:3191200-3196000	Weak transcription	Brain Substantia Nigra	brain
29	chr4:3191200-3201400	Weak transcription	Psoas Muscle	Psoas
30	chr4:3191200-3201400	Weak transcription	NHDF-Ad	bronchial
31	chr4:3191200-3203400	Weak transcription	Fetal Heart	heart
32	chr4:3191200-3208600	Weak transcription	A549	lung
33	chr4:3191400-3196600	Weak transcription	Brain Cingulate Gyrus	brain
34	chr4:3191400-3197400	Weak transcription	Colonic Mucosa	Colon
35	chr4:3191600-3196200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr4:3191600-3196400	Weak transcription	Fetal Brain Male	brain
37	chr4:3191600-3196800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr4:3191600-3199200	Weak transcription	HSMMtube	muscle
39	chr4:3191600-3201400	Weak transcription	NH-A	brain
40	chr4:3191600-3203600	Weak transcription	K562	blood
41	chr4:3191800-3197400	Weak transcription	NHLF	lung
42	chr4:3191800-3197600	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr4:3191800-3207800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:3191800-3208200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr4:3191800-3211600	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr4:3192000-3196000	Weak transcription	Fetal Lung	lung
47	chr4:3192000-3196200	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr4:3192000-3201400	Weak transcription	Colon Smooth Muscle	Colon
49	chr4:3192200-3196800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr4:3192200-3198600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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