Variant report

Variant	rs182638892
Chromosome Location	chr6:28191077-28191078
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:28184931..28189194-chr6:28190077..28194573,12	MCF-7	breast:
2	chr6:28182735..28195387-chr6:28315960..28325841,32	K562	blood:
3	chr6:28188764..28191744-chr6:28301995..28304592,2	MCF-7	breast:
4	chr6:28184789..28191313-chr6:28230652..28235913,7	K562	blood:
5	chr6:28189695..28192033-chr6:28349571..28352462,4	K562	blood:
6	chr6:28186460..28191177-chr6:28246836..28252039,7	K562	blood:
7	chr6:28047206..28049069-chr6:28188430..28191262,2	K562	blood:
8	chr6:28127881..28130043-chr6:28189652..28192231,2	K562	blood:
9	chr6:28183629..28195178-chr6:28316250..28325659,29	K562	blood:
10	chr6:28100317..28107200-chr6:28184436..28191088,8	MCF-7	breast:
11	chr6:28102806..28106129-chr6:28190797..28194598,4	K562	blood:
12	chr6:28102723..28113786-chr6:28183725..28194756,41	K562	blood:
13	chr6:28184339..28187958-chr6:28190844..28194750,7	MCF-7	breast:
14	chr6:28182366..28191375-chr6:28300021..28306741,17	K562	blood:
15	chr6:28163458..28166230-chr6:28188324..28191413,3	K562	blood:
16	chr6:28190987..28192829-chr6:28194559..28196499,2	MCF-7	breast:
17	chr6:28108043..28113786-chr6:28190485..28194607,10	K562	blood:
18	chr6:28188391..28191172-chr6:28347437..28349201,2	K562	blood:

No data

No data

No data

Variant related genes	Relation type
ENSG00000226314	Chromatin interaction
ENSG00000198315	Chromatin interaction
ENSG00000197062	Chromatin interaction
ENSG00000235109	Chromatin interaction
ENSG00000261839	Chromatin interaction
ENSG00000137185	Chromatin interaction
ENSG00000269293	Chromatin interaction
ENSG00000189298	Chromatin interaction
ENSG00000176933	Chromatin interaction
ENSG00000197279	Chromatin interaction
ENSG00000272009	Chromatin interaction
ENSG00000137338	Chromatin interaction

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830620	chr6:28173997-28348033	Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
2	esv2634712	chr6:28189671-28191361	Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:28186600-28192400	Weak transcription	Spleen	Spleen
2	chr6:28187000-28192400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr6:28187000-28192400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr6:28187200-28192000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr6:28187200-28192000	Weak transcription	HMEC	breast
6	chr6:28187200-28192200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:28187400-28192000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr6:28187400-28192000	Weak transcription	Hela-S3	cervix
9	chr6:28188200-28191200	Weak transcription	Placenta	Placenta
10	chr6:28188600-28192400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr6:28188800-28192000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr6:28188800-28192000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr6:28190000-28192400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr6:28190200-28192000	Weak transcription	K562	blood
15	chr6:28190800-28192200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:28191000-28192000	Weak transcription	NHEK	skin
17	chr6:28191000-28192200	Weak transcription	HUVEC	blood vessel

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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