Variant report

Variant	rs189532972
Chromosome Location	chr10:49912194-49912195
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:49905425..49907287-chr10:49911171..49913733,2	MCF-7	breast:
2	chr10:49907771..49909890-chr10:49911982..49914593,2	K562	blood:
3	chr10:49906264..49908604-chr10:49911628..49913491,2	MCF-7	breast:

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv895372	chr10:49576878-49933488	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1049259	chr10:49901984-49924310	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv895373	chr10:49911737-49933488	Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49897000-49918200	Genic enhancers	Primary B cells from peripheral blood	blood
2	chr10:49907400-49917800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr10:49907600-49912200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:49908200-49922800	Weak transcription	Spleen	Spleen
5	chr10:49909600-49912200	Enhancers	Fetal Stomach	stomach
6	chr10:49909800-49912400	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr10:49910000-49914000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
8	chr10:49910200-49913200	Enhancers	Fetal Lung	lung
9	chr10:49910600-49912200	Weak transcription	Esophagus	oesophagus
10	chr10:49910600-49912200	Weak transcription	Fetal Heart	heart
11	chr10:49910800-49912200	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr10:49910800-49917800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr10:49911000-49917800	Weak transcription	Primary hematopoietic stem cells	blood
14	chr10:49911000-49917800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr10:49911400-49913400	Enhancers	Placenta	Placenta
16	chr10:49911400-49913800	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr10:49911400-49914200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr10:49911600-49912400	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr10:49911600-49913400	Strong transcription	Primary B cells from cord blood	blood
20	chr10:49911800-49912600	Enhancers	Fetal Muscle Leg	muscle
21	chr10:49911800-49913000	Genic enhancers	GM12878-XiMat	blood
22	chr10:49911800-49913200	Enhancers	Left Ventricle	heart
23	chr10:49912000-49912600	Enhancers	Right Ventricle	heart
24	chr10:49912000-49912800	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr10:49912000-49913200	Enhancers	Lung	lung
26	chr10:49912000-49913200	Enhancers	Sigmoid Colon	Sigmoid Colon

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