Variant report

Variant	rs565207894
Chromosome Location	chr6:149765115-149765116
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:149757368..149759713-chr6:149765073..149766703,2	K562	blood:
2	chr6:149763319..149765484-chr6:149839894..149842239,2	MCF-7	breast:
3	chr6:149763379..149766103-chr6:149776553..149779366,2	MCF-7	breast:
4	chr6:149764839..149766396-chr6:149774052..149775951,2	MCF-7	breast:
5	chr6:149763441..149766003-chr6:149768583..149771236,2	K562	blood:

Variant related genes	Relation type
ENSG00000178199	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530444	chr6:149654540-149848997	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv470866	chr6:149744632-149806552	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv5533	chr6:149748047-149793072	Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv464076	chr6:149755695-149798835	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv604846	chr6:149755695-149798835	ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv3406755	chr6:149763459-149768057	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv3368142	chr6:149764359-149767257	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	esv3358632	chr6:149764809-149767607	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv2276365	chr6:149765080-149765483	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 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	chr6:149753400-149770000	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr6:149753600-149768400	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr6:149753600-149769600	Weak transcription	Primary B cells from peripheral blood	blood
4	chr6:149760600-149766600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr6:149760800-149765800	Weak transcription	GM12878-XiMat	blood
6	chr6:149761600-149769600	Weak transcription	Primary B cells from cord blood	blood
7	chr6:149762600-149770800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:149762800-149771000	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr6:149763200-149765800	Weak transcription	Right Ventricle	heart
10	chr6:149763200-149770000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr6:149763200-149771000	Weak transcription	Fetal Intestine Small	intestine
12	chr6:149763200-149771400	Weak transcription	Pancreas	Pancrea
13	chr6:149763400-149766000	Enhancers	HepG2	liver
14	chr6:149764000-149765200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr6:149764200-149765200	Bivalent Enhancer	Adipose Nuclei	Adipose
16	chr6:149764200-149765200	Enhancers	Brain Hippocampus Middle	brain
17	chr6:149764200-149765200	Enhancers	Fetal Lung	lung
18	chr6:149764200-149765200	Enhancers	Ovary	ovary
19	chr6:149764400-149765200	Enhancers	Brain Anterior Caudate	brain
20	chr6:149764400-149765200	Enhancers	Brain Cingulate Gyrus	brain
21	chr6:149764400-149765200	Enhancers	Brain Substantia Nigra	brain
22	chr6:149764400-149765200	Enhancers	Fetal Stomach	stomach
23	chr6:149764400-149765400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr6:149764400-149765400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr6:149764600-149765200	Bivalent Enhancer	Fetal Muscle Leg	muscle
26	chr6:149764600-149768600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
27	chr6:149764800-149765200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr6:149764800-149765200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
29	chr6:149764800-149765600	Weak transcription	Right Atrium	heart
30	chr6:149764800-149771400	Weak transcription	Spleen	Spleen
31	chr6:149765000-149765800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr6:149765000-149766400	Weak transcription	Left Ventricle	heart

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