Variant report

Variant	rs6989247
Chromosome Location	chr8:104383219-104383220
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr8:104383183-104383614	K562	blood:	n/a	n/a

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:104309661..104313454-chr8:104382208..104385836,8	MCF-7	breast:
2	chr8:104381633..104383715-chr8:104424202..104427564,3	K562	blood:
3	chr8:104382282..104385358-chr8:104387344..104390689,3	K562	blood:
4	chr8:104382634..104385222-chr8:104394415..104397249,2	K562	blood:
5	chr8:104382707..104385620-chr8:104427062..104430016,2	MCF-7	breast:
6	chr8:104380544..104384762-chr8:104386449..104389451,3	K562	blood:
7	chr8:104382288..104384118-chr8:104384150..104386828,2	MCF-7	breast:
8	chr8:104382426..104384366-chr8:104426073..104428422,3	MCF-7	breast:

No data

Variant related genes	Relation type
CTHRC1	TF binding region
ENSG00000164934	Chromatin interaction
ENSG00000164933	Chromatin interaction
ENSG00000266289	Chromatin interaction
ENSG00000207399	Chromatin interaction
ENSG00000164932	Chromatin interaction
ENSG00000164930	Chromatin interaction
ENSG00000247081	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429931	chr8:104097396-104878014	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	nsv1020476	chr8:104312212-104924482	Genic enhancers Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv539704	chr8:104312212-104924482	Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv1016395	chr8:104327541-104473005	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv1023048	chr8:104355188-104872701	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
6	nsv539705	chr8:104355188-104872701	ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
7	nsv1021345	chr8:104361854-104879684	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
8	nsv1032085	chr8:104362187-104878345	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
9	nsv1033477	chr8:104369940-104439632	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
10	nsv539706	chr8:104369940-104439632	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
11	nsv1034183	chr8:104369940-104814008	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
12	nsv539707	chr8:104369940-104814008	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
13	esv2625329	chr8:104382650-104384243	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
14	nsv396392	chr8:104382900-104383219	Active TSS Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
15	esv1010448	chr8:104382904-104383223	Active TSS Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
16	esv1577681	chr8:104382914-104383234	Weak transcription Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104357800-104383400	Weak transcription	Aorta	Aorta
2	chr8:104377800-104383400	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr8:104378000-104383400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr8:104378000-104383400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr8:104381600-104383800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr8:104382400-104383400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:104382400-104383400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr8:104382600-104383400	Weak transcription	NH-A	brain
9	chr8:104382800-104383800	Active TSS	HepG2	liver
10	chr8:104382800-104384000	Active TSS	A549	lung
11	chr8:104382800-104384200	Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr8:104382800-104384200	Active TSS	K562	blood
13	chr8:104383000-104384400	Weak transcription	Dnd41	blood
14	chr8:104383200-104383400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr8:104383200-104383400	Active TSS	Primary B cells from cord blood	blood
16	chr8:104383200-104383400	Bivalent/Poised TSS	Primary T cells fromperipheralblood	blood
17	chr8:104383200-104383400	Enhancers	Primary hematopoietic stem cells	blood
18	chr8:104383200-104383400	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr8:104383200-104383400	Bivalent/Poised TSS	Primary T helper cells PMA-I stimulated	--
20	chr8:104383200-104383400	Bivalent/Poised TSS	Primary T helper cells fromperipheralblood	blood
21	chr8:104383200-104383400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr8:104383200-104383400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr8:104383200-104383400	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr8:104383200-104383400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr8:104383200-104383400	Active TSS	Adipose Nuclei	Adipose
26	chr8:104383200-104383400	Active TSS	Fetal Stomach	stomach
27	chr8:104383200-104383400	Active TSS	Fetal Thymus	thymus
28	chr8:104383200-104383400	Enhancers	Right Ventricle	heart
29	chr8:104383200-104383400	Enhancers	HMEC	breast
30	chr8:104383200-104383600	Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr8:104383200-104383800	Active TSS	HUES64 Cell Line	embryonic stem cell
32	chr8:104383200-104383800	Active TSS	Rectal Mucosa Donor 29	rectum
33	chr8:104383200-104384000	Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr8:104383200-104384000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
35	chr8:104383200-104384000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr8:104383200-104384000	Bivalent/Poised TSS	Fetal Intestine Small	intestine
37	chr8:104383200-104384200	Active TSS	Primary T cells from cord blood	blood
38	chr8:104383200-104384200	Active TSS	Thymus	Thymus
39	chr8:104383200-104384400	Bivalent/Poised TSS	Fetal Brain Female	brain
40	chr8:104383200-104384400	Bivalent/Poised TSS	NHEK	skin

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