Variant report

Variant	rs363138
Chromosome Location	chr4:3177480-3177481
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:3173185..3175409-chr4:3176697..3178512,2	MCF-7	breast:
2	chr4:3168255..3170056-chr4:3176089..3177701,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10000252	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs10002065	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs10006977	1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10009229	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10009935	1.00[CEU][hapmap]
rs10010375	1.00[CEU][hapmap]
rs10011127	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10011241	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs10011412	1.00[CEU][hapmap]
rs10014333	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10016755	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs10030079	1.00[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs10034313	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10222986	1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13111546	1.00[AFR][1000 genomes]
rs1419036	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs16843857	0.93[EUR][1000 genomes]
rs16843866	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs16843869	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2471343	1.00[CEU][hapmap]
rs2515931	1.00[CEU][hapmap]
rs2515934	1.00[CEU][hapmap]
rs28387056	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28393280	0.87[EUR][1000 genomes]
rs28580164	0.93[EUR][1000 genomes]
rs28583552	0.90[EUR][1000 genomes]
rs28634516	0.93[EUR][1000 genomes]
rs28652828	0.84[EUR][1000 genomes]
rs28660254	0.93[EUR][1000 genomes]
rs28670335	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28696693	0.81[EUR][1000 genomes]
rs28707127	1.00[AFR][1000 genomes]
rs28718346	0.80[EUR][1000 genomes]
rs28755900	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3025799	1.00[AFR][1000 genomes]
rs3025836	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4346595	0.87[EUR][1000 genomes]
rs6830019	0.87[EUR][1000 genomes]
rs6835897	0.87[EUR][1000 genomes]
rs7436457	0.87[EUR][1000 genomes]
rs7664480	0.87[EUR][1000 genomes]
rs7693317	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs9291159	1.00[CEU][hapmap]
rs9991144	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs9994689	1.00[EUR][1000 genomes]
rs9995782	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9996075	0.87[EUR][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:127 , 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	chr4:3162600-3182200	Weak transcription	Small Intestine	intestine
4	chr4:3163000-3182000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr4:3167800-3203400	Strong transcription	Primary B cells from peripheral blood	blood
6	chr4:3168000-3180800	Strong transcription	Fetal Stomach	stomach
7	chr4:3168000-3182600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr4:3168000-3191800	Strong transcription	Primary T cells fromperipheralblood	blood
9	chr4:3168000-3192600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr4:3168000-3197600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr4:3168000-3202800	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr4:3168000-3203000	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr4:3170000-3208800	Weak transcription	Stomach Mucosa	stomach
14	chr4:3170200-3181200	Weak transcription	K562	blood
15	chr4:3170200-3185000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr4:3170600-3182200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr4:3171200-3186600	Strong transcription	GM12878-XiMat	blood
18	chr4:3171200-3197600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr4:3171400-3178000	Strong transcription	Fetal Muscle Trunk	muscle
20	chr4:3171400-3187200	Strong transcription	Primary B cells from cord blood	blood
21	chr4:3171400-3192800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr4:3171600-3178200	Strong transcription	Fetal Muscle Leg	muscle
23	chr4:3171600-3192800	Strong transcription	Primary T cells from cord blood	blood
24	chr4:3171600-3193600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr4:3171800-3180800	Strong transcription	Duodenum Smooth Muscle	Duodenum
26	chr4:3172000-3180000	Strong transcription	HepG2	liver
27	chr4:3172000-3192000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr4:3172000-3202800	Strong transcription	Duodenum Mucosa	Duodenum
29	chr4:3172200-3178000	Strong transcription	Fetal Intestine Small	intestine
30	chr4:3172200-3180400	Strong transcription	Liver	Liver
31	chr4:3172200-3193000	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr4:3172200-3195400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr4:3172400-3199800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:3172400-3238800	Strong transcription	HUES64 Cell Line	embryonic stem cell
35	chr4:3172600-3192400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr4:3172800-3202800	Strong transcription	Rectal Mucosa Donor 29	rectum
37	chr4:3173000-3181200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr4:3173000-3192600	Strong transcription	Primary T helper cells PMA-I stimulated	--
39	chr4:3173000-3193000	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr4:3173200-3182600	Strong transcription	Dnd41	blood
41	chr4:3173400-3178200	Strong transcription	Fetal Intestine Large	intestine
42	chr4:3173400-3180800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr4:3173400-3188800	Strong transcription	Sigmoid Colon	Sigmoid Colon
44	chr4:3173600-3177600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
45	chr4:3173600-3177600	Strong transcription	Brain Angular Gyrus	brain
46	chr4:3173600-3177800	Strong transcription	Brain Anterior Caudate	brain
47	chr4:3173600-3177800	Strong transcription	Brain Hippocampus Middle	brain
48	chr4:3173600-3177800	Strong transcription	Colon Smooth Muscle	Colon
49	chr4:3173600-3178000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr4:3173600-3178200	Strong transcription	Brain Cingulate Gyrus	brain

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