Variant report

Variant	rs17149190
Chromosome Location	chr11:68359185-68359186
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:68350724..68355507-chr11:68355875..68359661,5	K562	blood:
2	chr11:68356995..68359552-chr11:68362485..68365524,4	K562	blood:
3	chr11:68357372..68360145-chr11:68668136..68670562,2	MCF-7	breast:
4	chr11:68341428..68343456-chr11:68357720..68359630,3	K562	blood:
5	chr11:68350011..68354393-chr11:68355875..68359494,4	K562	blood:

Variant related genes	Relation type
ENSG00000110075	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1139093	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17149152	1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs17149156	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17149166	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17149176	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.88[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17149182	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58497241	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60142486	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3431317	chr11:68282676-68411867	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv3478641	chr11:68282679-68411856	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	esv3478652	chr11:68282679-68411856	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	esv3425206	chr11:68282708-68411817	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
5	esv3511614	chr11:68282726-68411806	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	esv3511615	chr11:68282726-68411806	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
7	esv3348204	chr11:68282891-68411839	Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
8	nsv832195	chr11:68286383-68474611	Strong transcription Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
9	nsv430403	chr11:68297201-68448324	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:68299200-68384000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr11:68304000-68384400	Strong transcription	Rectal Mucosa Donor 29	rectum
3	chr11:68309400-68384800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:68317000-68384200	Strong transcription	Fetal Muscle Trunk	muscle
5	chr11:68317600-68383600	Strong transcription	Placenta	Placenta
6	chr11:68318000-68383800	Strong transcription	Fetal Thymus	thymus
7	chr11:68318000-68384000	Strong transcription	Primary T cells fromperipheralblood	blood
8	chr11:68318200-68384200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr11:68318600-68384600	Strong transcription	Primary B cells from cord blood	blood
10	chr11:68319200-68384200	Strong transcription	Duodenum Mucosa	Duodenum
11	chr11:68319800-68384000	Strong transcription	Liver	Liver
12	chr11:68321000-68361800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr11:68324400-68362000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr11:68324600-68361600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr11:68325600-68361200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr11:68328800-68362000	Strong transcription	Sigmoid Colon	Sigmoid Colon
17	chr11:68328800-68380600	Strong transcription	Fetal Muscle Leg	muscle
18	chr11:68329200-68384400	Strong transcription	Rectal Mucosa Donor 31	rectum
19	chr11:68333800-68384000	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr11:68333800-68384400	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr11:68336800-68383800	Strong transcription	Dnd41	blood
22	chr11:68337000-68384000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr11:68337200-68360600	Strong transcription	Primary T cells from cord blood	blood
24	chr11:68337200-68381000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr11:68337200-68384000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr11:68337400-68361800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr11:68337400-68383400	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr11:68337400-68383800	Strong transcription	Primary T helper cells PMA-I stimulated	--
29	chr11:68337600-68384600	Strong transcription	Primary neutrophils fromperipheralblood	blood
30	chr11:68337800-68361600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr11:68338800-68360600	Strong transcription	Thymus	Thymus
32	chr11:68341800-68383400	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr11:68342200-68385800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr11:68347000-68360200	Strong transcription	Fetal Stomach	stomach
35	chr11:68347400-68360200	Strong transcription	Fetal Intestine Small	intestine
36	chr11:68347800-68374800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr11:68351000-68383200	Strong transcription	Fetal Intestine Large	intestine
38	chr11:68351200-68362000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr11:68351200-68373000	Strong transcription	Primary T helper naive cells from peripheral blood	blood
40	chr11:68351200-68383800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr11:68351600-68360400	Strong transcription	HUVEC	blood vessel
42	chr11:68351600-68360800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr11:68351600-68361600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr11:68351600-68366200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr11:68351600-68384200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:68351800-68360200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr11:68351800-68361800	Strong transcription	H1 Cell Line	embryonic stem cell
48	chr11:68351800-68362000	Strong transcription	Osteobl	bone
49	chr11:68351800-68363400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr11:68351800-68382800	Strong transcription	Primary B cells from peripheral blood	blood

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