Variant report

Variant	rs1200108
Chromosome Location	chr1:169057969-169057970
allele	A/G
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:5)
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	CEBPB	chr1:169057873-169058161	HepG2	liver:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:169055830..169060702-chr1:169073415..169077056,5	MCF-7	breast:
2	chr1:169057841..169060357-chr1:169064186..169066001,2	K562	blood:
3	chr1:169053133..169065213-chr1:169070028..169077898,15	MCF-7	breast:
4	chr1:169057728..169060027-chr1:169075441..169077080,2	K562	blood:
5	chr1:169057319..169059341-chr1:169064126..169065686,2	K562	blood:

No data

Variant related genes	Relation type
LINC00970	TF binding region
ENSG00000237707	Chromatin interaction
ENSG00000143153	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1040506	0.90[EUR][1000 genomes]
rs1200089	0.88[CEU][hapmap];1.00[CHB][hapmap];0.87[EUR][1000 genomes]
rs1200092	0.87[EUR][1000 genomes]
rs1200097	0.90[EUR][1000 genomes]
rs1200099	0.91[EUR][1000 genomes]
rs1200103	0.91[EUR][1000 genomes]
rs1200105	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1200106	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1200114	0.92[CEU][hapmap];0.95[EUR][1000 genomes]
rs1200115	0.92[CEU][hapmap]
rs1320973	1.00[CHB][hapmap]
rs1575041	0.88[CEU][hapmap];1.00[CHB][hapmap];0.87[EUR][1000 genomes]
rs1575042	0.88[CEU][hapmap];1.00[CHB][hapmap];0.87[EUR][1000 genomes]
rs2982459	0.87[EUR][1000 genomes]
rs2982461	0.87[EUR][1000 genomes]
rs3007369	0.86[EUR][1000 genomes]
rs3007370	0.88[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes]
rs4656175	0.91[EUR][1000 genomes]
rs909926	1.00[JPT][hapmap]

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	nsv869415	chr1:168467284-169153863	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
2	esv3522071	chr1:168978325-169339044	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
3	esv3522072	chr1:168978325-169339044	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
4	nsv831858	chr1:169022383-169179068	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169054800-169058600	Enhancers	Fetal Intestine Large	intestine
2	chr1:169055000-169058000	Enhancers	Fetal Intestine Small	intestine
3	chr1:169055200-169058600	Enhancers	Brain Angular Gyrus	brain
4	chr1:169055200-169062200	Enhancers	Brain Anterior Caudate	brain
5	chr1:169055400-169060400	Enhancers	Brain Substantia Nigra	brain
6	chr1:169055800-169058000	Enhancers	Duodenum Smooth Muscle	Duodenum
7	chr1:169055800-169058000	Enhancers	Right Ventricle	heart
8	chr1:169055800-169058200	Enhancers	Colon Smooth Muscle	Colon
9	chr1:169056000-169058200	Enhancers	Rectal Smooth Muscle	rectum
10	chr1:169056200-169062600	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr1:169056400-169058400	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr1:169056400-169060200	Weak transcription	Right Atrium	heart
13	chr1:169056400-169062800	Enhancers	Brain Cingulate Gyrus	brain
14	chr1:169056600-169058600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:169056600-169063400	Enhancers	Brain Hippocampus Middle	brain
16	chr1:169056800-169058600	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr1:169056800-169059200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr1:169056800-169060400	Enhancers	Fetal Heart	heart
19	chr1:169056800-169060400	Weak transcription	Fetal Muscle Leg	muscle
20	chr1:169056800-169064000	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr1:169057200-169058200	Weak transcription	Stomach Mucosa	stomach
22	chr1:169057200-169064000	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr1:169057600-169058000	Weak transcription	Duodenum Mucosa	Duodenum
24	chr1:169057600-169058600	Weak transcription	Pancreas	Pancrea
25	chr1:169057600-169058800	Enhancers	Left Ventricle	heart
26	chr1:169057600-169058800	Enhancers	HepG2	liver
27	chr1:169057800-169058400	Enhancers	Hela-S3	cervix
28	chr1:169057800-169059800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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