Variant report

Variant	rs2585085
Chromosome Location	chr15:57311511-57311512
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:57209175..57210784-chr15:57308733..57311658,2	K562	blood:
2	chr15:57310993..57315176-chr15:57315668..57319705,4	K562	blood:

Variant related genes	Relation type
ENSG00000137871	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs1652733	1.00[YRI][hapmap]
rs2243575	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2435894	1.00[AMR][1000 genomes]
rs2435899	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs2435900	0.82[AFR][1000 genomes]
rs2435901	0.87[AFR][1000 genomes]
rs2435904	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs2439923	0.87[AFR][1000 genomes]
rs2439924	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs2566841	0.82[AFR][1000 genomes]
rs2566847	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2566852	0.87[AFR][1000 genomes]
rs2585074	1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs2585079	1.00[AMR][1000 genomes]
rs2585092	0.87[AFR][1000 genomes]
rs2585095	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2585100	0.82[AFR][1000 genomes]
rs2585101	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2585109	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2585111	0.87[AFR][1000 genomes]
rs2585113	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2585122	1.00[YRI][hapmap]
rs2593213	0.93[AFR][1000 genomes]
rs2593214	0.87[AFR][1000 genomes]
rs2593227	0.87[AFR][1000 genomes]
rs2593245	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs2593247	0.86[AFR][1000 genomes]
rs2593253	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs2615234	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2615239	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs2615245	0.86[AFR][1000 genomes]
rs2615247	1.00[AMR][1000 genomes]
rs2703581	1.00[AMR][1000 genomes]
rs2703585	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs2703603	0.87[AFR][1000 genomes]
rs2703606	0.87[AFR][1000 genomes]
rs2703609	0.93[AFR][1000 genomes]
rs2703611	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2703617	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs2703618	0.82[AFR][1000 genomes]
rs2703621	1.00[AMR][1000 genomes]
rs2703622	0.87[AFR][1000 genomes]
rs2703625	0.87[AFR][1000 genomes]
rs2733169	0.93[AFR][1000 genomes]
rs2733173	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs2733175	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2733184	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2733186	0.87[AFR][1000 genomes]
rs2733190	0.87[AFR][1000 genomes]
rs2733308	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2733338	1.00[AMR][1000 genomes]
rs2920271	0.87[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1042486	chr15:57094598-57505992	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv542393	chr15:57115116-57341363	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv1052052	chr15:57232111-57344561	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv542394	chr15:57232111-57344561	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv904251	chr15:57241970-57575916	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:57276200-57313400	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr15:57277000-57313400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr15:57282000-57315000	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr15:57282200-57315200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr15:57286200-57312000	Weak transcription	HSMM	muscle
6	chr15:57286200-57314800	Weak transcription	Dnd41	blood
7	chr15:57289600-57315200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr15:57289600-57315600	Weak transcription	Fetal Muscle Leg	muscle
9	chr15:57289800-57315600	Weak transcription	Primary B cells from cord blood	blood
10	chr15:57294400-57311600	Weak transcription	GM12878-XiMat	blood
11	chr15:57295200-57313600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr15:57296600-57313200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:57297200-57316800	Weak transcription	Fetal Stomach	stomach
14	chr15:57299200-57316000	Weak transcription	Right Ventricle	heart
15	chr15:57299200-57317200	Weak transcription	Esophagus	oesophagus
16	chr15:57300200-57313800	Strong transcription	Fetal Thymus	thymus
17	chr15:57303600-57317600	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr15:57305000-57311800	Weak transcription	Aorta	Aorta
19	chr15:57305000-57312000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr15:57305000-57313400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr15:57305000-57313400	Weak transcription	Right Atrium	heart
22	chr15:57306400-57312400	Enhancers	Placenta	Placenta
23	chr15:57307000-57311600	Weak transcription	NHLF	lung
24	chr15:57307600-57312200	Enhancers	Brain Anterior Caudate	brain
25	chr15:57307600-57312400	Enhancers	A549	lung
26	chr15:57307600-57312800	Enhancers	Brain Substantia Nigra	brain
27	chr15:57307800-57312600	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr15:57307800-57313400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr15:57307800-57323400	Weak transcription	Pancreas	Pancrea
30	chr15:57308000-57317400	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr15:57308000-57328000	Weak transcription	Gastric	stomach
32	chr15:57308200-57311800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr15:57308400-57311800	Weak transcription	HUVEC	blood vessel
34	chr15:57308600-57311600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr15:57308600-57311600	Weak transcription	NH-A	brain
36	chr15:57308800-57311800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr15:57308800-57323400	Weak transcription	Small Intestine	intestine
38	chr15:57309200-57323400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr15:57309400-57311600	Weak transcription	Liver	Liver
40	chr15:57309400-57311800	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr15:57309400-57315000	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr15:57309400-57323000	Weak transcription	Primary hematopoietic stem cells	blood
43	chr15:57309400-57334600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr15:57309600-57311600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr15:57309600-57312800	Enhancers	Osteobl	bone
46	chr15:57309600-57313200	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr15:57309600-57316000	Weak transcription	Fetal Intestine Small	intestine
48	chr15:57309600-57317200	Weak transcription	Psoas Muscle	Psoas
49	chr15:57309600-57323200	Weak transcription	Thymus	Thymus
50	chr15:57310000-57312600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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