Variant report

Variant	rs35619616
Chromosome Location	chr15:31224230-31224231
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:31223541..31225627-chr15:31225836..31228644,2	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1043251	0.94[ASN][1000 genomes]
rs10467918	0.88[ASN][1000 genomes]
rs1088471	0.82[ASN][1000 genomes]
rs1088475	0.82[ASN][1000 genomes]
rs12903674	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12914843	0.81[EUR][1000 genomes]
rs2140733	0.82[ASN][1000 genomes]
rs2691682	0.82[ASN][1000 genomes]
rs2955782	0.82[ASN][1000 genomes]
rs2955789	0.88[ASN][1000 genomes]
rs34178381	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4779792	0.88[ASN][1000 genomes]
rs565	1.00[ASN][1000 genomes]
rs6493352	0.94[ASN][1000 genomes]
rs71474639	0.83[AFR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7171212	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8026711	0.88[ASN][1000 genomes]
rs811304	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427955	chr15:30467980-31273174	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv531138	chr15:30653877-31609679	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
3	nsv916936	chr15:30921917-31337510	Active TSS Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv525795	chr15:30936285-31324531	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv533434	chr15:30938215-31244225	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
6	nsv903831	chr15:30986051-31723279	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
7	nsv1046874	chr15:31008133-31294654	Enhancers Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
8	nsv1054147	chr15:31014507-31972706	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
9	nsv542306	chr15:31014507-31972706	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
10	nsv832951	chr15:31131239-31304469	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
11	nsv1039037	chr15:31140415-31277268	Strong transcription ZNF genes & repeats Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
12	nsv542309	chr15:31140415-31277268	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
13	nsv1036018	chr15:31140415-31544888	Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
14	nsv521842	chr15:31140700-31272670	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
15	nsv903834	chr15:31179534-31293774	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
16	esv33507	chr15:31183324-31471023	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
17	nsv832952	chr15:31204426-31333998	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS 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	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs35619616	FAN1	cis	Whole Blood	GTEx
rs35619616	MTMR15	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31200400-31242200	Strong transcription	Primary T cells from cord blood	blood
2	chr15:31200600-31254800	Strong transcription	Primary T helper cells fromperipheralblood	blood
3	chr15:31201200-31241400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr15:31214800-31230600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr15:31215200-31238600	Weak transcription	Fetal Heart	heart
6	chr15:31215200-31241000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:31215800-31236600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr15:31216000-31241600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr15:31216600-31224800	Weak transcription	Right Atrium	heart
10	chr15:31216600-31225000	Strong transcription	HUES64 Cell Line	embryonic stem cell
11	chr15:31216600-31245800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr15:31217200-31224800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
13	chr15:31217800-31228600	Weak transcription	Fetal Kidney	kidney
14	chr15:31218200-31228400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr15:31220000-31228800	Weak transcription	HSMM	muscle
16	chr15:31220000-31233800	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr15:31220200-31226800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr15:31221000-31246800	Strong transcription	Cortex derived primary cultured neurospheres	brain
19	chr15:31221600-31225200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr15:31221600-31230600	Weak transcription	K562	blood
21	chr15:31222400-31224600	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr15:31222600-31241000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr15:31222800-31229000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr15:31222800-31232600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr15:31222800-31233000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr15:31223000-31226000	Weak transcription	Rectal Smooth Muscle	rectum
27	chr15:31223000-31226600	Weak transcription	Primary B cells from peripheral blood	blood
28	chr15:31223000-31226600	Weak transcription	Fetal Thymus	thymus
29	chr15:31223000-31228600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr15:31223000-31228800	Weak transcription	Colonic Mucosa	Colon
31	chr15:31223000-31229000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr15:31223000-31229200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr15:31223000-31229400	Weak transcription	HSMMtube	muscle
34	chr15:31223000-31232400	Weak transcription	Stomach Mucosa	stomach
35	chr15:31223200-31225200	Weak transcription	GM12878-XiMat	blood
36	chr15:31223200-31225200	Weak transcription	NHEK	skin
37	chr15:31223200-31225400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr15:31223200-31226000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr15:31223200-31226000	Weak transcription	Fetal Intestine Small	intestine
40	chr15:31223200-31226000	Weak transcription	Lung	lung
41	chr15:31223200-31226200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr15:31223200-31227000	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr15:31223200-31227200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr15:31223200-31227200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr15:31223200-31228400	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr15:31223200-31228400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr15:31223200-31228400	Weak transcription	Spleen	Spleen
48	chr15:31223200-31228400	Weak transcription	NHDF-Ad	bronchial
49	chr15:31223200-31228800	Weak transcription	Hela-S3	cervix
50	chr15:31223200-31229000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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