Variant report

Variant	rs1216537
Chromosome Location	chr1:113421402-113421403
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:113415161..113418488-chr1:113420570..113424322,4	K562	blood:
2	chr1:113411911..113414258-chr1:113419696..113422107,2	MCF-7	breast:
3	chr1:113420602..113421810-chr1:113584981..113585927,5	K562	blood:
4	chr1:113420012..113422020-chr1:113615413..113617603,2	K562	blood:
5	chr1:113255487..113258161-chr1:113420887..113423423,3	K562	blood:
6	chr1:113421355..113423469-chr1:113497371..113499587,2	MCF-7	breast:
7	chr1:113415018..113417156-chr1:113420570..113423546,3	K562	blood:

Variant related genes	Relation type
ENSG00000155367	Chromatin interaction
ENSG00000238198	Chromatin interaction
ENSG00000226419	Chromatin interaction
ENSG00000198799	Chromatin interaction
ENSG00000155380	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1235629	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1237670	0.88[CEU][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17440299	0.81[CEU][hapmap]
rs17493313	0.81[CEU][hapmap]
rs2149036	0.81[CEU][hapmap]
rs2360008	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2996294	1.00[ASW][hapmap];0.95[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2996389	0.95[CEU][hapmap];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2996391	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2996392	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3849174	0.81[CEU][hapmap]
rs4839270	0.81[CEU][hapmap]
rs4839272	0.81[CEU][hapmap]
rs7518984	0.81[CEU][hapmap]
rs7536532	0.81[CEU][hapmap]
rs7550843	0.81[CEU][hapmap]
rs7552903	0.81[CEU][hapmap]
rs9429505	0.81[CEU][hapmap]
rs9429709	0.81[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002971	chr1:112924725-113740584	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
2	nsv535059	chr1:112924725-113740584	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
3	nsv1010276	chr1:113123932-113740584	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised 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 miRNA target site	158 gene(s)	inside rSNPs	diseases
4	nsv533295	chr1:113167645-113589588	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
5	nsv1012119	chr1:113214869-113759081	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
6	nsv535060	chr1:113214869-113759081	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
7	nsv529238	chr1:113229946-113759080	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
8	nsv818378	chr1:113263711-113434818	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
9	nsv1008434	chr1:113288282-113447426	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
10	nsv997426	chr1:113288282-113639507	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
11	nsv1004102	chr1:113295805-113551210	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
12	esv3399982	chr1:113358580-113542255	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
13	nsv999915	chr1:113360145-113684833	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats 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	69 gene(s)	inside rSNPs	diseases
14	esv18293	chr1:113375437-113852815	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
15	esv3362439	chr1:113376621-113450321	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription 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

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs1216537	OVGP1	cis	cerebellum	SCAN
rs1216537	DDX20	cis	cerebellum	SCAN
rs1216537	LRIG2	cis	cerebellum	SCAN
rs1216537	SLC16A1	Cis_1M	lymphoblastoid	RTeQTL
rs1216537	ATP1A1	cis	cerebellum	SCAN
rs1216537	GNAI3	cis	cerebellum	SCAN

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:113415000-113424600	Weak transcription	Right Atrium	heart
2	chr1:113415600-113423400	Weak transcription	Osteobl	bone
3	chr1:113415800-113422000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:113415800-113423200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr1:113416000-113423200	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr1:113416000-113424600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr1:113417000-113424400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:113417200-113421600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:113417200-113423600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr1:113417800-113423600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:113418000-113423400	Weak transcription	NHEK	skin
12	chr1:113418000-113423600	Weak transcription	HMEC	breast
13	chr1:113420400-113421600	Enhancers	Brain Hippocampus Middle	brain
14	chr1:113420600-113423000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr1:113420800-113421600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr1:113420800-113423800	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr1:113421000-113421600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr1:113421000-113421600	Enhancers	Colonic Mucosa	Colon
19	chr1:113421000-113421600	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr1:113421000-113423000	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr1:113421200-113421600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:113421200-113422000	Weak transcription	Placenta	Placenta
23	chr1:113421200-113422400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr1:113421200-113423200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr1:113421200-113423800	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr1:113421200-113424400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr1:113421200-113424400	Weak transcription	Brain Cingulate Gyrus	brain
28	chr1:113421200-113424600	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr1:113421400-113421600	Enhancers	K562	blood
30	chr1:113421400-113422200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr1:113421400-113423400	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr1:113421400-113423400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr1:113421400-113423400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr1:113421400-113423400	Weak transcription	Brain Substantia Nigra	brain
35	chr1:113421400-113424400	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr1:113421400-113424600	Weak transcription	Fetal Brain Female	brain
37	chr1:113421400-113424800	Weak transcription	Brain Angular Gyrus	brain
38	chr1:113421400-113435200	Weak transcription	Fetal Heart	heart

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