Variant report

Variant	rs367741012
Chromosome Location	chr8:121655289-121655290
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:31)
CpG islands
(count:0)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr8:121655220-121655370	A549	lung:	n/a	n/a
2	ZNF143	chr8:121655171-121655430	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr8:121655240-121655390	MCF-7	breast:	n/a	n/a
4	CTCF	chr8:121655280-121655430	GM12873	blood:	n/a	n/a
5	CTCF	chr8:121655280-121655430	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr8:121655265-121655404	K562	blood:	n/a	n/a
7	CTCF	chr8:121655160-121655310	HFF-Myc	foreskin:	n/a	n/a
8	CTCF	chr8:121655280-121655430	GM12870	blood:	n/a	n/a
9	CTCF	chr8:121655260-121655410	GM12869	blood:	n/a	n/a
10	CTCF	chr8:121655240-121655390	GM12872	blood:	n/a	n/a
11	CTCF	chr8:121655240-121655390	HMF	breast:	n/a	n/a
12	CTCF	chr8:121655220-121655370	GM12874	blood:	n/a	n/a
13	CTCF	chr8:121655220-121655370	HCT-116	colon:	n/a	n/a
14	CTCF	chr8:121655200-121655350	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr8:121655160-121655310	BE2_C	brain:	n/a	n/a
16	CTCF	chr8:121655220-121655370	HCPEpiC	choroid plexus:	n/a	n/a
17	POLR2A	chr8:121655199-121655457	HepG2	liver:	n/a	n/a
18	CTCF	chr8:121655280-121655430	HFF-Myc	foreskin:	n/a	n/a
19	CTCF	chr8:121655260-121655410	HEK293	kidney:	n/a	n/a
20	CTCF	chr8:121655260-121655410	GM12864	blood:	n/a	n/a
21	CTCF	chr8:121655260-121655410	NB4	blood:	n/a	n/a
22	CTCF	chr8:121655100-121655390	GM12865	blood:	n/a	n/a
23	CTCF	chr8:121655180-121655330	HPAF	blood vessel:	n/a	n/a
24	CTCF	chr8:121655254-121655397	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr8:121655287-121655355	GM12892	blood:	n/a	n/a
26	CTCF	chr8:121655280-121655430	HepG2	liver:	n/a	n/a
27	CTCF	chr8:121655277-121655371	GM19238	blood:	n/a	n/a
28	CTCF	chr8:121655240-121655390	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr8:121655220-121655370	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr8:121655260-121655410	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr8:121655260-121655410	K562	blood:	n/a	n/a

No data

Variant related genes	Relation type
ENSG00000250290	TF binding region

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv6369	chr8:121654665-121699920	ZNF genes & repeats Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:121613200-121668000	Weak transcription	Pancreas	Pancrea
2	chr8:121628600-121673200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr8:121644200-121666800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr8:121644800-121664400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr8:121644800-121664400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr8:121644800-121674800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr8:121645000-121664400	Weak transcription	NHLF	lung
8	chr8:121645000-121666400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr8:121645000-121673000	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr8:121645200-121655400	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr8:121645200-121665200	Weak transcription	Primary B cells from cord blood	blood
12	chr8:121645400-121662400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr8:121645600-121662400	Weak transcription	Primary T cells from cord blood	blood
14	chr8:121646400-121666800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr8:121653200-121656400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr8:121653200-121656400	Strong transcription	Liver	Liver
17	chr8:121653400-121655400	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr8:121653600-121655400	Enhancers	Placenta	Placenta
19	chr8:121653600-121656400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr8:121654200-121655800	Strong transcription	HepG2	liver
21	chr8:121654400-121656800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr8:121655000-121655600	ZNF genes & repeats	Fetal Muscle Trunk	muscle
23	chr8:121655200-121655400	ZNF genes & repeats	HSMM	muscle
24	chr8:121655200-121655600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
25	chr8:121655200-121655600	ZNF genes & repeats	HSMMtube	muscle
26	chr8:121655200-121663200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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