Variant report

Variant	rs371788126
Chromosome Location	chr6:3987306-3987307
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:3985992..3988806-chr6:4017298..4019133,2	MCF-7	breast:
2	chr6:3980920..3982632-chr6:3985928..3988379,2	MCF-7	breast:
3	chr6:3985295..3987675-chr6:3989539..3991361,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf146-7	chr6:3987194-3987711	NONHSAT107259

Variant related genes	Relation type
ENSG00000272248	Chromatin interaction

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	nsv532020	chr6:3417520-4140257	Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv1022968	chr6:3862744-4272502	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	nsv538106	chr6:3862744-4272502	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
4	esv1800199	chr6:3986611-4014872	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:3964800-3987400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr6:3976400-3990800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr6:3978600-3991000	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr6:3978600-3991000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr6:3978800-3991000	Weak transcription	Primary B cells from peripheral blood	blood
6	chr6:3978800-3991000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr6:3978800-3991000	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr6:3979000-3990600	Weak transcription	Colon Smooth Muscle	Colon
9	chr6:3979000-3990800	Weak transcription	HSMM	muscle
10	chr6:3979000-3991000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr6:3979000-4003200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr6:3979200-3990600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr6:3979200-3991000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr6:3979400-3990800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr6:3980400-3987600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr6:3980600-3987600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:3980600-4003600	Weak transcription	Primary B cells from cord blood	blood
18	chr6:3980800-3990800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr6:3982200-3987400	Weak transcription	Fetal Lung	lung
20	chr6:3982400-3990600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:3983000-3991000	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr6:3983800-3990800	Weak transcription	Ovary	ovary
23	chr6:3985400-4011000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr6:3985800-3990800	Weak transcription	Rectal Smooth Muscle	rectum
25	chr6:3986600-3987400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr6:3986600-3987400	Enhancers	Right Atrium	heart
27	chr6:3986600-3987600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr6:3986600-3987800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr6:3986600-3987800	Strong transcription	Primary T cells from cord blood	blood
30	chr6:3986600-3987800	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr6:3986600-3987800	Enhancers	HepG2	liver
32	chr6:3986600-3988000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr6:3986600-3988000	Enhancers	HUVEC	blood vessel
34	chr6:3986800-3987400	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr6:3986800-3987400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr6:3986800-3987400	Enhancers	Small Intestine	intestine
37	chr6:3986800-3987600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr6:3986800-3987600	Enhancers	Placenta	Placenta
39	chr6:3986800-3987600	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr6:3986800-3987800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr6:3986800-3987800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr6:3986800-3987800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr6:3986800-3987800	Enhancers	Adipose Nuclei	Adipose
44	chr6:3986800-3987800	Enhancers	Fetal Intestine Small	intestine
45	chr6:3986800-3987800	Enhancers	Left Ventricle	heart
46	chr6:3986800-3987800	Enhancers	Pancreas	Pancrea
47	chr6:3986800-3987800	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr6:3986800-3987800	Enhancers	NH-A	brain
49	chr6:3986800-3987800	Enhancers	NHDF-Ad	bronchial
50	chr6:3986800-3987800	Enhancers	Osteobl	bone

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