Variant report

Variant	rs537698889
Chromosome Location	chr1:226006567-226006568
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:226000008..226002119-chr1:226004674..226006661,2	MCF-7	breast:
2	chr1:225964451..225968253-chr1:226004384..226007160,4	K562	blood:
3	chr1:225965233..225968253-chr1:226004557..226007160,3	K562	blood:
4	chr1:225965293..225968073-chr1:226004323..226008130,4	MCF-7	breast:
5	chr1:226004168..226006685-chr1:226076298..226078625,2	K562	blood:
6	chr1:226004660..226006754-chr1:226008430..226011315,2	K562	blood:
7	chr1:225991700..225994994-chr1:226006068..226008999,3	K562	blood:
8	chr1:225999526..226002981-chr1:226005681..226008708,3	MCF-7	breast:
9	chr1:226004285..226007407-chr1:226008778..226014958,9	K562	blood:
10	chr1:226005737..226007634-chr1:226011731..226014314,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000143742	Chromatin interaction
ENSG00000243709	Chromatin interaction
ENSG00000143819	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1795046	chr1:225874059-226091150	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	esv1834932	chr1:225874059-226091150	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	esv1834948	chr1:225874059-226214882	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers 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 miRNA target site	60 gene(s)	inside rSNPs	diseases
4	nsv524126	chr1:225973777-226210653	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv947519	chr1:225998770-226034631	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	esv3419876	chr1:226006558-226007066	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225998400-226007800	Enhancers	Spleen	Spleen
2	chr1:225999200-226006600	Enhancers	Psoas Muscle	Psoas
3	chr1:225999400-226006600	Enhancers	Right Ventricle	heart
4	chr1:225999400-226007800	Enhancers	Left Ventricle	heart
5	chr1:226000000-226006600	Enhancers	Brain Substantia Nigra	brain
6	chr1:226000000-226019400	Weak transcription	Fetal Brain Female	brain
7	chr1:226000400-226007400	Enhancers	Brain Anterior Caudate	brain
8	chr1:226000400-226015800	Enhancers	Ovary	ovary
9	chr1:226001800-226006800	Enhancers	Rectal Smooth Muscle	rectum
10	chr1:226001800-226010200	Enhancers	HepG2	liver
11	chr1:226001800-226019200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr1:226003200-226007600	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chr1:226003400-226006600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr1:226003800-226008800	Enhancers	Fetal Stomach	stomach
15	chr1:226004000-226007600	Enhancers	Pancreas	Pancrea
16	chr1:226004200-226006600	Enhancers	Brain Angular Gyrus	brain
17	chr1:226004600-226006600	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr1:226004600-226009400	Enhancers	Fetal Lung	lung
19	chr1:226004800-226007800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr1:226005200-226006800	Enhancers	Right Atrium	heart
21	chr1:226005200-226008600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:226005400-226007200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:226005400-226007800	Enhancers	Adipose Nuclei	Adipose
24	chr1:226005600-226012000	Weak transcription	Fetal Intestine Large	intestine
25	chr1:226005600-226019400	Weak transcription	Brain Germinal Matrix	brain
26	chr1:226005800-226007200	Strong transcription	Fetal Intestine Small	intestine
27	chr1:226005800-226007800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr1:226005800-226008200	Enhancers	Liver	Liver
29	chr1:226005800-226008600	Enhancers	Colon Smooth Muscle	Colon
30	chr1:226005800-226009400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr1:226005800-226010400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr1:226005800-226011600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr1:226005800-226012000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:226005800-226012400	Weak transcription	Placenta	Placenta
35	chr1:226005800-226013000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr1:226005800-226013400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr1:226005800-226019200	Weak transcription	NHLF	lung
38	chr1:226005800-226019400	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr1:226005800-226019400	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr1:226006000-226007200	Weak transcription	Fetal Heart	heart
41	chr1:226006000-226008400	Weak transcription	HMEC	breast
42	chr1:226006000-226011200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr1:226006200-226007200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:226006200-226007200	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr1:226006200-226007200	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr1:226006200-226007600	Weak transcription	Fetal Muscle Trunk	muscle
47	chr1:226006200-226008200	Weak transcription	K562	blood
48	chr1:226006200-226008400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr1:226006200-226009400	Enhancers	Stomach Mucosa	stomach
50	chr1:226006200-226010400	Genic enhancers	A549	lung

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