Variant report

Variant	rs16870732
Chromosome Location	chr7:3132116-3132117
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12540595	0.89[AFR][1000 genomes]
rs67787789	0.98[ASN][1000 genomes]
rs73050252	0.90[ASN][1000 genomes]
rs73050258	0.91[ASN][1000 genomes]
rs73050267	0.90[ASN][1000 genomes]
rs7456058	0.91[ASN][1000 genomes]
rs7788891	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv605873	chr7:2920067-3204177	Bivalent Enhancer Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv1026476	chr7:2965034-3311344	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv538656	chr7:2965034-3311344	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv464260	chr7:2966138-3315572	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv605874	chr7:2966138-3315572	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv1018287	chr7:2967524-3298539	Genic enhancers Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv538657	chr7:2967524-3298539	Bivalent/Poised TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	nsv887319	chr7:3099853-3134593	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv887320	chr7:3110446-3134593	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv605875	chr7:3117801-3134593	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv1020680	chr7:3125512-3204521	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
12	nsv1027945	chr7:3125512-3208071	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
13	nsv1015656	chr7:3131821-3321353	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3128800-3132200	Enhancers	Primary T cells fromperipheralblood	blood
2	chr7:3128800-3134200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr7:3128800-3134400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr7:3129400-3134200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr7:3129600-3134600	Enhancers	Fetal Thymus	thymus
6	chr7:3130200-3134400	Enhancers	Primary B cells from peripheral blood	blood
7	chr7:3130200-3134400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr7:3130600-3133200	Enhancers	Primary hematopoietic stem cells	blood
9	chr7:3130600-3134200	Enhancers	Primary B cells from cord blood	blood
10	chr7:3131000-3132400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
11	chr7:3131000-3132600	Enhancers	Spleen	Spleen
12	chr7:3131000-3133200	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr7:3131200-3132200	Weak transcription	Thymus	Thymus
14	chr7:3131200-3134000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:3131200-3134400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr7:3131400-3132200	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr7:3131400-3132400	Flanking Active TSS	Primary T cells from cord blood	blood
18	chr7:3131400-3132400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
19	chr7:3131600-3132200	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr7:3131600-3132400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
21	chr7:3131600-3132600	Enhancers	Dnd41	blood
22	chr7:3131800-3132200	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr7:3131800-3132400	Enhancers	Adipose Nuclei	Adipose
24	chr7:3131800-3132600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
25	chr7:3131800-3132600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
26	chr7:3131800-3132600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
27	chr7:3131800-3132800	Enhancers	Duodenum Mucosa	Duodenum
28	chr7:3131800-3133000	Enhancers	GM12878-XiMat	blood
29	chr7:3131800-3134400	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr7:3132000-3132200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
31	chr7:3132000-3132800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr7:3132000-3133800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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