Variant report

Variant	rs4397881
Chromosome Location	chr11:74867699-74867700
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NR2F2	chr11:74866680-74867712	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:74867339..74870278-chr11:74875624..74878251,3	K562	blood:
2	chr11:74860782..74862620-chr11:74866728..74869676,2	MCF-7	breast:
3	chr11:74866771..74870278-chr11:74874697..74878251,4	K562	blood:
4	chr11:74860426..74862138-chr11:74866873..74869626,2	K562	blood:

Variant related genes	Relation type
SLCO2B1	TF binding region
ENSG00000137491	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10899077	0.88[AMR][1000 genomes]
rs10899078	0.91[CHB][hapmap];0.86[JPT][hapmap];0.82[MEX][hapmap];0.88[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10899079	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11236348	0.80[AMR][1000 genomes]
rs11236349	0.80[AMR][1000 genomes]
rs11236351	0.80[AMR][1000 genomes]
rs11236352	0.80[AMR][1000 genomes]
rs11236353	0.80[AMR][1000 genomes]
rs11236356	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11236357	0.91[CHB][hapmap];0.81[GIH][hapmap];0.91[JPT][hapmap];0.91[MEX][hapmap];0.92[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs11236358	0.96[ASN][1000 genomes]
rs11236361	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11236365	0.81[JPT][hapmap];0.81[AMR][1000 genomes]
rs11827488	0.92[CEU][hapmap]
rs12361277	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12422149	0.81[JPT][hapmap]
rs17133732	0.88[CEU][hapmap]
rs3740839	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.95[MEX][hapmap];0.81[MKK][hapmap];0.92[TSI][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4100076	1.00[CEU][hapmap];0.91[CHB][hapmap];0.88[GIH][hapmap];0.82[LWK][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4944073	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.90[GIH][hapmap];0.95[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4944074	0.81[JPT][hapmap];0.82[MEX][hapmap];0.85[AMR][1000 genomes]
rs4944974	0.89[CEU][hapmap];0.84[TSI][hapmap]
rs4944990	0.81[CHB][hapmap]
rs4944991	0.81[CHB][hapmap];0.82[MEX][hapmap];0.88[AMR][1000 genomes]
rs4944992	0.91[CHB][hapmap];0.86[JPT][hapmap];0.82[MEX][hapmap];0.88[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4944993	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4944994	0.91[CHB][hapmap];0.81[GIH][hapmap];0.91[JPT][hapmap];0.87[MEX][hapmap];0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs57073688	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59633704	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6592602	0.89[CEU][hapmap];0.92[TSI][hapmap]
rs67904312	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67947132	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7125268	0.81[JPT][hapmap]
rs72996586	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72998525	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs881217	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs949069	0.87[CHB][hapmap];0.91[JPT][hapmap];0.82[MEX][hapmap];0.81[ASN][1000 genomes]

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	nsv897919	chr11:74862391-74875501	Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74861200-74868400	Active TSS	Brain Hippocampus Middle	brain
2	chr11:74863600-74885600	Weak transcription	Colon Smooth Muscle	Colon
3	chr11:74864200-74898400	Weak transcription	Esophagus	oesophagus
4	chr11:74864800-74868600	Enhancers	Pancreas	Pancrea
5	chr11:74864800-74870400	Enhancers	Fetal Intestine Large	intestine
6	chr11:74865000-74872000	Enhancers	Placenta	Placenta
7	chr11:74865400-74868000	Enhancers	Fetal Muscle Leg	muscle
8	chr11:74865400-74868200	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr11:74865400-74868200	Enhancers	Stomach Mucosa	stomach
10	chr11:74865400-74868600	Enhancers	Fetal Stomach	stomach
11	chr11:74865400-74868800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:74865400-74868800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr11:74866000-74869000	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr11:74866000-74869600	Weak transcription	Brain Substantia Nigra	brain
15	chr11:74866200-74873000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr11:74866400-74868000	Weak transcription	Small Intestine	intestine
17	chr11:74866400-74869400	Enhancers	Fetal Intestine Small	intestine
18	chr11:74866400-74869600	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr11:74866400-74870000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:74866400-74871000	Weak transcription	Spleen	Spleen
21	chr11:74866400-74873000	Weak transcription	Fetal Thymus	thymus
22	chr11:74866800-74870400	Weak transcription	Left Ventricle	heart
23	chr11:74867000-74867800	Flanking Active TSS	HepG2	liver
24	chr11:74867000-74869000	Enhancers	Colonic Mucosa	Colon
25	chr11:74867200-74868200	Weak transcription	Brain Anterior Caudate	brain
26	chr11:74867400-74870200	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr11:74867400-74870800	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr11:74867400-74870800	Weak transcription	A549	lung
29	chr11:74867400-74873200	Weak transcription	Brain Cingulate Gyrus	brain
30	chr11:74867600-74867800	Enhancers	Duodenum Mucosa	Duodenum
31	chr11:74867600-74868000	Enhancers	Liver	Liver
32	chr11:74867600-74868400	Weak transcription	Lung	lung
33	chr11:74867600-74868400	Weak transcription	Ovary	ovary
34	chr11:74867600-74868600	Enhancers	Rectal Mucosa Donor 29	rectum
35	chr11:74867600-74869200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr11:74867600-74869800	Weak transcription	Fetal Muscle Trunk	muscle
37	chr11:74867600-74869800	Weak transcription	Gastric	stomach
38	chr11:74867600-74870000	Weak transcription	Right Ventricle	heart
39	chr11:74867600-74870200	Weak transcription	Adipose Nuclei	Adipose
40	chr11:74867600-74870400	Weak transcription	Rectal Smooth Muscle	rectum
41	chr11:74867600-74870400	Weak transcription	Right Atrium	heart
42	chr11:74867600-74870800	Weak transcription	Stomach Smooth Muscle	stomach
43	chr11:74867600-74875000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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