Variant report

Variant	rs1218564
Chromosome Location	chr1:154818152-154818153
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:154807688..154810280-chr1:154815696..154818405,2	K562	blood:
2	chr1:154812878..154815262-chr1:154817032..154818549,2	K562	blood:
3	chr1:154793548..154796604-chr1:154817553..154820667,3	MCF-7	breast:

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs1218559	0.83[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1218560	0.86[AFR][1000 genomes]
rs1218561	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1218563	0.85[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][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	nsv532579	chr1:154548165-155262692	Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	575 gene(s)	inside rSNPs	diseases
2	nsv427797	chr1:154559115-154933717	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv432931	chr1:154794318-154855055	Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:154803200-154824600	Enhancers	Fetal Brain Male	brain
2	chr1:154808400-154823600	Enhancers	Fetal Muscle Leg	muscle
3	chr1:154812000-154818600	Enhancers	Fetal Stomach	stomach
4	chr1:154812000-154822000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr1:154812400-154824400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:154812600-154822000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr1:154813000-154818600	Weak transcription	Colon Smooth Muscle	Colon
8	chr1:154813200-154818400	Weak transcription	Rectal Smooth Muscle	rectum
9	chr1:154813200-154818600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr1:154813200-154818600	Weak transcription	Fetal Kidney	kidney
11	chr1:154813600-154818400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:154813600-154818400	Weak transcription	Lung	lung
13	chr1:154813800-154821600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr1:154813800-154822600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr1:154814000-154818600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:154814800-154820400	Weak transcription	Pancreas	Pancrea
17	chr1:154815800-154820200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr1:154815800-154823200	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr1:154816800-154818400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:154816800-154819000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr1:154816800-154819200	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr1:154816800-154820200	Enhancers	Fetal Brain Female	brain
23	chr1:154817000-154818400	Enhancers	GM12878-XiMat	blood
24	chr1:154817000-154818600	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr1:154817000-154818800	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr1:154817000-154819200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr1:154817000-154820200	Enhancers	Brain Germinal Matrix	brain
28	chr1:154817600-154818400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
29	chr1:154817600-154819000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
30	chr1:154817600-154819400	Enhancers	Fetal Intestine Small	intestine
31	chr1:154817600-154819400	Enhancers	Fetal Thymus	thymus
32	chr1:154817600-154820200	Enhancers	Brain Anterior Caudate	brain
33	chr1:154817600-154820200	Enhancers	Brain Cingulate Gyrus	brain
34	chr1:154817600-154821200	Enhancers	Psoas Muscle	Psoas
35	chr1:154817800-154818200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
36	chr1:154817800-154818800	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr1:154817800-154818800	Enhancers	Right Ventricle	heart
38	chr1:154817800-154819000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr1:154817800-154819000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr1:154817800-154819000	Enhancers	Fetal Intestine Large	intestine
41	chr1:154817800-154819200	Enhancers	Primary hematopoietic stem cells	blood
42	chr1:154817800-154819200	Bivalent Enhancer	Placenta	Placenta
43	chr1:154817800-154819800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr1:154817800-154819800	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr1:154817800-154820200	Enhancers	Brain Angular Gyrus	brain
46	chr1:154817800-154823200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr1:154818000-154818400	Enhancers	Primary B cells from peripheral blood	blood
48	chr1:154818000-154818600	Enhancers	Right Atrium	heart
49	chr1:154818000-154818800	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr1:154818000-154819000	Enhancers	Fetal Lung	lung

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