Variant report

Variant	rs574749752
Chromosome Location	chr2:96679494-96679495
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:96678269..96680437-chr2:96873411..96875898,2	MCF-7	breast:
2	chr2:96674813..96677740-chr2:96678852..96681143,2	K562	blood:
3	chr2:96678462..96681368-chr2:96930331..96932535,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CIAO1-4	chr2:96679197-96679831	NONHSAT072533

Variant related genes	Relation type
ENSG00000135956	Chromatin interaction
ENSG00000084090	Chromatin interaction
ENSG00000204685	Chromatin interaction
ENSG00000231584	Chromatin interaction
ENSG00000144021	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3416818	chr2:96072529-96680708	Strong transcription Weak transcription Enhancers 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	43 gene(s)	inside rSNPs	diseases
2	nsv516044	chr2:96150959-96683378	Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv1003371	chr2:96326106-96684876	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv874666	chr2:96370571-96691125	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv1004486	chr2:96544604-96684876	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv874669	chr2:96547820-96691125	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv818073	chr2:96554851-96683378	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	esv1840487	chr2:96582807-96836512	Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
9	nsv870250	chr2:96610946-96739308	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
10	esv1837811	chr2:96622689-96730375	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
11	nsv874670	chr2:96637870-96693357	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	nsv874671	chr2:96637870-96727850	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
13	nsv874672	chr2:96637870-96809331	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
14	nsv874673	chr2:96647856-96825363	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
15	nsv874674	chr2:96651163-96741944	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
16	esv1836563	chr2:96669134-96730375	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
17	esv993391	chr2:96671521-96731854	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
18	nsv961454	chr2:96677855-96701857	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96675600-96691400	Weak transcription	Gastric	stomach
2	chr2:96675800-96689000	Weak transcription	Spleen	Spleen
3	chr2:96676400-96688400	Weak transcription	Colon Smooth Muscle	Colon
4	chr2:96677000-96680000	Weak transcription	Brain Germinal Matrix	brain
5	chr2:96677000-96681800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr2:96677000-96682000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr2:96677000-96682800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:96677000-96685000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:96677000-96686200	Weak transcription	Pancreas	Pancrea
10	chr2:96677000-96688200	Weak transcription	Fetal Muscle Trunk	muscle
11	chr2:96677000-96688200	Weak transcription	Fetal Muscle Leg	muscle
12	chr2:96677000-96688400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr2:96677000-96690200	Weak transcription	Right Ventricle	heart
14	chr2:96677000-96690400	Weak transcription	Fetal Intestine Small	intestine
15	chr2:96677200-96680400	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr2:96677200-96680400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr2:96677200-96688200	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr2:96677200-96688800	Weak transcription	Stomach Smooth Muscle	stomach
19	chr2:96677400-96684800	Weak transcription	Brain Angular Gyrus	brain
20	chr2:96678000-96679800	Enhancers	Brain Substantia Nigra	brain
21	chr2:96678400-96679800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr2:96678600-96679600	Enhancers	Brain Cingulate Gyrus	brain
23	chr2:96678600-96691000	Weak transcription	Left Ventricle	heart
24	chr2:96678800-96681600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr2:96678800-96682800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr2:96678800-96684800	Weak transcription	Brain Hippocampus Middle	brain
27	chr2:96678800-96685000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr2:96678800-96690800	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr2:96679000-96679800	Strong transcription	Fetal Stomach	stomach
30	chr2:96679400-96679800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr2:96679400-96679800	Genic enhancers	Brain Inferior Temporal Lobe	brain
32	chr2:96679400-96684800	Weak transcription	Brain Anterior Caudate	brain

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