Variant report

Variant	rs142456745
Chromosome Location	chr11:63677870-63677871
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:63673944..63681438-chr11:63681488..63685981,13	K562	blood:
2	chr11:63674570..63680304-chr11:63681753..63686803,9	MCF-7	breast:
3	chr11:63534031..63536529-chr11:63677173..63679815,2	K562	blood:
4	chr11:63603311..63612666-chr11:63664740..63679491,25	MCF-7	breast:

Variant related genes	Relation type
ENSG00000167771	Chromatin interaction
ENSG00000255651	Chromatin interaction
ENSG00000072518	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051171	chr11:62987064-63835715	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
2	nsv468589	chr11:63515752-63713239	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv555180	chr11:63515752-63713239	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	esv1839119	chr11:63615554-63680052	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv468590	chr11:63639881-63783352	Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv555181	chr11:63639881-63783352	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
7	nsv897629	chr11:63664882-63866959	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
8	nsv897630	chr11:63664882-63924446	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
9	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
10	nsv897632	chr11:63670787-63688693	Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
11	nsv897633	chr11:63670787-63691049	Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
12	nsv897634	chr11:63670787-63698538	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
13	nsv897635	chr11:63674926-63688693	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
14	nsv897636	chr11:63676067-63688693	Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
15	nsv897637	chr11:63676067-63691049	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
16	nsv897638	chr11:63676562-63688693	Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63658800-63678400	Strong transcription	Primary B cells from cord blood	blood
2	chr11:63659400-63678600	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr11:63659600-63680600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr11:63659800-63678000	Strong transcription	Rectal Mucosa Donor 31	rectum
5	chr11:63659800-63682400	Strong transcription	Fetal Intestine Large	intestine
6	chr11:63660800-63678000	Strong transcription	Primary B cells from peripheral blood	blood
7	chr11:63661000-63678000	Strong transcription	Liver	Liver
8	chr11:63661200-63678600	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr11:63661600-63678000	Strong transcription	Thymus	Thymus
10	chr11:63661600-63678000	Strong transcription	NHEK	skin
11	chr11:63662400-63679200	Strong transcription	Colonic Mucosa	Colon
12	chr11:63662400-63679200	Strong transcription	Gastric	stomach
13	chr11:63664000-63678600	Strong transcription	Primary T helper cells PMA-I stimulated	--
14	chr11:63664200-63678400	Strong transcription	Sigmoid Colon	Sigmoid Colon
15	chr11:63664200-63679200	Strong transcription	Primary T cells from cord blood	blood
16	chr11:63664400-63678800	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr11:63664400-63679200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr11:63664600-63680400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr11:63669600-63683200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr11:63670000-63683200	Weak transcription	K562	blood
21	chr11:63670000-63683400	Weak transcription	HSMM	muscle
22	chr11:63670800-63681600	Weak transcription	GM12878-XiMat	blood
23	chr11:63671000-63681800	Weak transcription	HUVEC	blood vessel
24	chr11:63671000-63683800	Weak transcription	NHDF-Ad	bronchial
25	chr11:63672200-63682600	Weak transcription	HepG2	liver
26	chr11:63672200-63682600	Weak transcription	NH-A	brain
27	chr11:63672400-63679400	Genic enhancers	Fetal Muscle Trunk	muscle
28	chr11:63672400-63683200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr11:63672400-63683800	Weak transcription	Psoas Muscle	Psoas
30	chr11:63672600-63679800	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr11:63673200-63678800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr11:63673200-63680400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr11:63673200-63682600	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr11:63673200-63683200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr11:63673400-63678000	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr11:63673800-63679000	Enhancers	H1 Cell Line	embryonic stem cell
37	chr11:63673800-63682800	Weak transcription	Osteobl	bone
38	chr11:63674000-63679200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr11:63674000-63679200	Genic enhancers	Fetal Stomach	stomach
40	chr11:63674400-63679200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr11:63674400-63679200	Genic enhancers	Fetal Muscle Leg	muscle
42	chr11:63674400-63679200	Genic enhancers	Placenta	Placenta
43	chr11:63674600-63678400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr11:63674600-63678600	Genic enhancers	Cortex derived primary cultured neurospheres	brain
45	chr11:63674600-63679000	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr11:63674600-63679200	Enhancers	Fetal Heart	heart
47	chr11:63674800-63679200	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr11:63674800-63679200	Strong transcription	Lung	lung
49	chr11:63675400-63679200	Genic enhancers	Fetal Brain Female	brain
50	chr11:63675800-63678800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood

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