Variant report

Variant	rs150292271
Chromosome Location	chr1:92060692-92060693
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:92060019..92063789-chr1:92065058..92070338,4	K562	blood:
2	chr1:92059728..92061441-chr1:92068842..92071690,2	K562	blood:
3	chr1:92056853..92058906-chr1:92058997..92061738,3	K562	blood:
4	chr1:92038932..92042320-chr1:92059008..92062228,3	K562	blood:
5	chr1:91999544..92001051-chr1:92060316..92062281,2	K562	blood:
6	chr1:92057409..92061312-chr1:92170673..92173610,3	K562	blood:

Variant related genes	Relation type
ENSG00000229067	Chromatin interaction

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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	nsv949516	chr1:91644418-92109261	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1009560	chr1:91897078-92270781	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv946071	chr1:92060669-92067233	Weak transcription Enhancers Bivalent Enhancer	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	chr1:92049600-92061600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:92051800-92067600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:92055000-92060800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr1:92055400-92061200	Enhancers	Ovary	ovary
5	chr1:92055600-92061400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:92055800-92076400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr1:92056000-92062200	Enhancers	Fetal Heart	heart
8	chr1:92057200-92070400	Weak transcription	Psoas Muscle	Psoas
9	chr1:92057600-92061600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr1:92057600-92063400	Enhancers	K562	blood
11	chr1:92057800-92061600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr1:92058400-92061800	Enhancers	Placenta	Placenta
13	chr1:92058800-92061400	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr1:92059600-92066200	Weak transcription	Fetal Stomach	stomach
15	chr1:92059600-92067200	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr1:92059800-92068800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr1:92060000-92060800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr1:92060000-92060800	Enhancers	Colon Smooth Muscle	Colon
19	chr1:92060000-92060800	Enhancers	Duodenum Smooth Muscle	Duodenum
20	chr1:92060000-92060800	Enhancers	Rectal Smooth Muscle	rectum
21	chr1:92060000-92060800	Enhancers	Right Atrium	heart
22	chr1:92060000-92060800	Enhancers	Stomach Smooth Muscle	stomach
23	chr1:92060600-92060800	Enhancers	Left Ventricle	heart
24	chr1:92060600-92061600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:92060600-92067200	Weak transcription	Lung	lung
26	chr1:92060600-92070200	Weak transcription	Right Ventricle	heart

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