Variant report

Variant	rs191401938
Chromosome Location	chr2:178536826-178536827
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:178536377..178538004-chr2:178556463..178558808,2	K562	blood:
2	chr2:178533626..178535228-chr2:178535564..178538374,2	K562	blood:

Extended variants
information (count: 5 )
Associated
traits (count: 0)

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	nsv999086	chr2:178262348-178773585	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv536055	chr2:178262348-178773585	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv583688	chr2:178427640-178540293	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv431812	chr2:178525371-178584470	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1007925	chr2:178535922-178577002	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:178531400-178540000	Weak transcription	K562	blood
2	chr2:178532800-178537000	Enhancers	Fetal Kidney	kidney
3	chr2:178532800-178538000	Weak transcription	HSMM	muscle
4	chr2:178534000-178537200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:178534200-178537000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr2:178534400-178537400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
7	chr2:178534800-178537000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:178534800-178537000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr2:178534800-178537200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
10	chr2:178535000-178544800	Weak transcription	Right Atrium	heart
11	chr2:178535400-178540000	Weak transcription	Liver	Liver
12	chr2:178535600-178537000	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr2:178535800-178537000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr2:178536000-178537200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
15	chr2:178536000-178540000	Weak transcription	Brain Substantia Nigra	brain
16	chr2:178536000-178540000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr2:178536000-178544600	Weak transcription	Psoas Muscle	Psoas
18	chr2:178536200-178537200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr2:178536200-178540200	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr2:178536200-178540200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr2:178536600-178537000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
22	chr2:178536600-178540400	Weak transcription	Fetal Stomach	stomach
23	chr2:178536600-178556000	Weak transcription	Pancreas	Pancrea
24	chr2:178536800-178537000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell

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