Variant report

Variant	rs7105097
Chromosome Location	chr11:72474816-72474817
allele	C/T
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	POLR2A	chr11:72474697-72474865	HepG2	liver:	n/a	n/a
2	PAX5	chr11:72474639-72475456	GM12878	blood:	n/a	chr11:72475052-72475069 chr11:72475059-72475068 chr11:72475050-72475068
3	PAX5	chr11:72474786-72475402	GM12878	blood:	n/a	chr11:72475052-72475069 chr11:72475059-72475068 chr11:72475050-72475068
4	PAX5	chr11:72474708-72475452	GM12878	blood:	n/a	chr11:72475052-72475069 chr11:72475059-72475068 chr11:72475050-72475068
5	POLR2A	chr11:72474697-72474853	K562	blood:	n/a	n/a
6	POLR2A	chr11:72474430-72474956	H1-neurons	neurons:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:72436033..72436583-chr11:72474182..72475033,2	MCF-7	breast:
2	chr11:72474113..72475649-chr11:72522703..72524985,2	MCF-7	breast:
3	chr11:72472551..72476853-chr11:72484240..72487215,3	MCF-7	breast:
4	chr11:72471822..72474020-chr11:72474362..72475948,2	MCF-7	breast:
5	chr11:72454556..72456545-chr11:72472426..72474862,2	K562	blood:
6	chr11:72468175..72472129-chr11:72473505..72476644,4	K562	blood:

Variant related genes	Relation type
ENSG00000202522	TF binding region
STARD10	TF binding region
ENSG00000214530	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs55651216	1.00[AMR][1000 genomes]
rs55806368	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55822003	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55970824	1.00[AMR][1000 genomes]
rs56088156	1.00[AMR][1000 genomes]
rs56294550	1.00[AMR][1000 genomes]
rs58387586	1.00[AMR][1000 genomes]
rs61139682	1.00[AMR][1000 genomes]

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	esv1806140	chr11:72268466-72546175	Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	77 gene(s)	inside rSNPs	diseases
2	esv3394774	chr11:72320884-72694077	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:72464200-72475200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr11:72464400-72475200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr11:72464400-72475200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr11:72464400-72479200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr11:72464400-72483600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:72464400-72491400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr11:72464600-72492000	Weak transcription	Primary hematopoietic stem cells	blood
8	chr11:72464800-72483200	Weak transcription	Fetal Thymus	thymus
9	chr11:72466000-72475200	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr11:72466200-72475200	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr11:72466200-72475200	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr11:72466200-72475200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr11:72470000-72491400	Weak transcription	Aorta	Aorta
14	chr11:72470200-72475000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr11:72470200-72482600	Weak transcription	Colon Smooth Muscle	Colon
16	chr11:72470400-72477400	Weak transcription	Esophagus	oesophagus
17	chr11:72470400-72479000	Weak transcription	Right Ventricle	heart
18	chr11:72470400-72482000	Weak transcription	Rectal Smooth Muscle	rectum
19	chr11:72470400-72482200	Weak transcription	Brain Angular Gyrus	brain
20	chr11:72470400-72482200	Weak transcription	Stomach Smooth Muscle	stomach
21	chr11:72470400-72486800	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr11:72470400-72491000	Weak transcription	Brain Germinal Matrix	brain
23	chr11:72470600-72475200	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr11:72470600-72477600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr11:72470600-72492000	Weak transcription	Primary T cells from cord blood	blood
26	chr11:72470800-72477200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr11:72470800-72479400	Weak transcription	Colonic Mucosa	Colon
28	chr11:72470800-72481800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr11:72470800-72482800	Weak transcription	Brain Cingulate Gyrus	brain
30	chr11:72470800-72483600	Weak transcription	Fetal Lung	lung
31	chr11:72470800-72483600	Weak transcription	Right Atrium	heart
32	chr11:72470800-72484200	Weak transcription	Fetal Brain Female	brain
33	chr11:72470800-72484400	Weak transcription	Ovary	ovary
34	chr11:72471000-72475400	Weak transcription	Fetal Muscle Trunk	muscle
35	chr11:72471000-72482400	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr11:72471000-72482400	Weak transcription	K562	blood
37	chr11:72472200-72475600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr11:72472200-72477600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr11:72472200-72481200	Genic enhancers	Fetal Intestine Small	intestine
40	chr11:72472200-72482200	Weak transcription	Brain Anterior Caudate	brain
41	chr11:72472200-72484400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr11:72472400-72477200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr11:72472800-72475200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr11:72472800-72482200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr11:72473400-72475400	Enhancers	Primary B cells from peripheral blood	blood
46	chr11:72473600-72475000	Enhancers	Spleen	Spleen
47	chr11:72473600-72475200	Genic enhancers	Liver	Liver
48	chr11:72473600-72475800	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr11:72473600-72476400	Strong transcription	HepG2	liver
50	chr11:72473600-72480200	Genic enhancers	Fetal Intestine Large	intestine

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