Variant report

Variant	rs182345627
Chromosome Location	chr6:13247870-13247871
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:13246618..13250195-chr6:13274363..13276198,3	K562	blood:
2	chr6:13243200..13244860-chr6:13246425..13248696,2	MCF-7	breast:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432849	chr6:13225077-13253733	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv532021	chr6:13232627-13805381	Active TSS Genic enhancers Strong transcription Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
3	esv1815942	chr6:13235495-13250588	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv1817130	chr6:13235495-13250588	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv1830412	chr6:13235495-13250588	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv1832850	chr6:13235495-13250588	Strong transcription Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv1846185	chr6:13235495-13250588	Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv1848354	chr6:13235495-13250588	Bivalent Enhancer Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv1028533	chr6:13239059-13484814	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer 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	23 gene(s)	inside rSNPs	diseases
10	nsv538136	chr6:13239059-13484814	Strong transcription Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
11	nsv981320	chr6:13247460-13253055	Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13229400-13248200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr6:13230600-13253400	Weak transcription	Spleen	Spleen
3	chr6:13230800-13248000	Weak transcription	Fetal Muscle Leg	muscle
4	chr6:13231200-13248200	Weak transcription	Fetal Stomach	stomach
5	chr6:13233200-13256000	Weak transcription	Right Ventricle	heart
6	chr6:13234600-13267200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr6:13235200-13248200	Weak transcription	HSMMtube	muscle
8	chr6:13236000-13248000	Weak transcription	Brain Germinal Matrix	brain
9	chr6:13237600-13252800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr6:13239000-13253200	Weak transcription	Aorta	Aorta
11	chr6:13240000-13248000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr6:13240200-13248000	Weak transcription	Brain Angular Gyrus	brain
13	chr6:13240200-13248000	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr6:13240200-13248200	Weak transcription	Brain Anterior Caudate	brain
15	chr6:13240200-13251200	Weak transcription	Left Ventricle	heart
16	chr6:13240400-13248000	Weak transcription	Brain Hippocampus Middle	brain
17	chr6:13241200-13250200	Weak transcription	Fetal Heart	heart
18	chr6:13241600-13251200	Weak transcription	Stomach Smooth Muscle	stomach
19	chr6:13242800-13248200	Weak transcription	Lung	lung
20	chr6:13242800-13256000	Weak transcription	Pancreas	Pancrea
21	chr6:13243200-13248200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr6:13243600-13248000	Weak transcription	HepG2	liver
23	chr6:13244000-13250400	Weak transcription	Primary hematopoietic stem cells	blood
24	chr6:13244400-13248000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr6:13244400-13250200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr6:13245000-13248000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr6:13245000-13250200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr6:13245600-13248200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr6:13246600-13249800	Enhancers	Fetal Brain Male	brain
30	chr6:13247800-13248800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr6:13247800-13249600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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