Variant report

Variant	rs1597320
Chromosome Location	chr14:81211175-81211176
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1016507	0.88[CHB][hapmap];1.00[YRI][hapmap]
rs12431821	0.87[CHB][hapmap];0.87[YRI][hapmap]
rs12878945	0.82[JPT][hapmap]
rs12880014	0.96[CEU][hapmap];0.93[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12888082	0.88[CHB][hapmap];1.00[YRI][hapmap]
rs12891585	0.92[CHB][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes]
rs12896065	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1458993	0.88[CHB][hapmap]
rs17542615	0.87[CHB][hapmap]
rs17542712	0.83[JPT][hapmap]
rs17613911	1.00[CEU][hapmap];0.88[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17614081	0.88[CHB][hapmap];0.80[EUR][1000 genomes]
rs1992973	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2246617	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs228120	1.00[YRI][hapmap]
rs2371413	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2371416	0.82[CHB][hapmap]
rs2371457	1.00[YRI][hapmap]
rs2590480	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2596118	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34848301	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4523859	0.88[CHB][hapmap];1.00[YRI][hapmap]
rs4903948	1.00[YRI][hapmap]
rs6574605	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7141434	1.00[CEU][hapmap];0.88[CHB][hapmap];0.94[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7145233	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7148618	0.87[CHB][hapmap];1.00[YRI][hapmap]
rs7154132	1.00[YRI][hapmap]
rs759916	0.81[CHB][hapmap];1.00[YRI][hapmap]
rs8005809	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8006864	1.00[YRI][hapmap]
rs8016601	1.00[YRI][hapmap]
rs8017943	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8021137	1.00[YRI][hapmap]
rs8022411	1.00[YRI][hapmap]
rs8023233	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv565290	chr14:81085129-81230117	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1035295	chr14:81180999-81236636	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81182800-81224600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr14:81185800-81221200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr14:81192800-81221000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr14:81192800-81305400	Weak transcription	Primary B cells from cord blood	blood
5	chr14:81193000-81220800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr14:81195400-81223000	Weak transcription	Pancreas	Pancrea
7	chr14:81197400-81212800	Weak transcription	A549	lung
8	chr14:81198200-81220000	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr14:81199800-81248600	Weak transcription	Primary T cells from cord blood	blood
10	chr14:81203800-81229000	Weak transcription	Left Ventricle	heart
11	chr14:81204600-81217600	Strong transcription	Dnd41	blood
12	chr14:81205000-81261000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr14:81205200-81222800	Weak transcription	HMEC	breast
14	chr14:81206400-81226800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr14:81207200-81232600	Weak transcription	Brain Cingulate Gyrus	brain
16	chr14:81207600-81226200	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr14:81207600-81230800	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr14:81207600-81265400	Weak transcription	Primary hematopoietic stem cells	blood
19	chr14:81208000-81215000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr14:81208400-81240400	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr14:81208600-81211600	Strong transcription	Thymus	Thymus
22	chr14:81208800-81232400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr14:81209400-81227800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr14:81209400-81229000	Weak transcription	Fetal Lung	lung
25	chr14:81209600-81248200	Weak transcription	HSMM	muscle
26	chr14:81210600-81220400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr14:81210600-81223400	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr14:81210600-81230400	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr14:81211000-81211600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr14:81211000-81211600	Strong transcription	Fetal Thymus	thymus

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