Variant report

Variant	rs567718700
Chromosome Location	chr11:75092358-75092359
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:75092274..75095773-chr11:75096854..75099923,3	K562	blood:
2	chr11:75090369..75092612-chr11:75094388..75097255,4	MCF-7	breast:
3	chr11:75090671..75094563-chr11:75095690..75099742,4	K562	blood:
4	chr11:75092197..75094711-chr11:75109480..75112038,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000206941	Chromatin interaction
ENSG00000149273	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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	nsv1041640	chr11:74945824-75174688	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	94 gene(s)	inside rSNPs	diseases
2	nsv832211	chr11:74945839-75106125	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
3	nsv897920	chr11:75087520-75181249	Genic enhancers Bivalent Enhancer Active TSS Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	esv993873	chr11:75090965-75093952	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75081200-75095200	Weak transcription	Dnd41	blood
2	chr11:75083600-75094200	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr11:75083800-75099400	Weak transcription	Right Atrium	heart
4	chr11:75087400-75099400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr11:75089800-75092400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr11:75089800-75092600	Enhancers	Fetal Intestine Large	intestine
7	chr11:75089800-75093000	Enhancers	Fetal Intestine Small	intestine
8	chr11:75090200-75092400	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr11:75090200-75092800	Enhancers	Rectal Mucosa Donor 29	rectum
10	chr11:75090400-75096000	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr11:75090800-75093000	Enhancers	Placenta	Placenta
12	chr11:75091000-75092400	Enhancers	Fetal Heart	heart
13	chr11:75091000-75092400	Enhancers	Fetal Muscle Leg	muscle
14	chr11:75091200-75093000	Enhancers	Stomach Mucosa	stomach
15	chr11:75091400-75092400	Enhancers	Placenta Amnion	Placenta Amnion
16	chr11:75091400-75092400	Enhancers	A549	lung
17	chr11:75091400-75094200	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr11:75091400-75096000	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr11:75091600-75092400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr11:75091600-75092400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr11:75091600-75092400	Enhancers	Primary hematopoietic stem cells	blood
22	chr11:75091600-75092400	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr11:75091600-75092400	Enhancers	K562	blood
24	chr11:75091600-75092600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr11:75091600-75092600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr11:75091800-75092400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr11:75091800-75092400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr11:75091800-75092400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr11:75091800-75092400	Enhancers	Colonic Mucosa	Colon
30	chr11:75091800-75092400	Enhancers	Esophagus	oesophagus
31	chr11:75091800-75092400	Enhancers	Fetal Muscle Trunk	muscle
32	chr11:75091800-75092400	Enhancers	Spleen	Spleen
33	chr11:75091800-75093000	Enhancers	Lung	lung
34	chr11:75092000-75092400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr11:75092000-75092400	Enhancers	Adipose Nuclei	Adipose
36	chr11:75092000-75092400	Enhancers	Colon Smooth Muscle	Colon
37	chr11:75092000-75092400	Enhancers	Small Intestine	intestine
38	chr11:75092000-75093600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr11:75092000-75094200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr11:75092000-75095400	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr11:75092000-75098200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr11:75092000-75099400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr11:75092200-75093200	Bivalent Enhancer	HepG2	liver
44	chr11:75092200-75094200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr11:75092200-75094200	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr11:75092200-75095400	Weak transcription	Liver	Liver
47	chr11:75092200-75095400	Weak transcription	Duodenum Mucosa	Duodenum
48	chr11:75092200-75095400	Weak transcription	Fetal Stomach	stomach
49	chr11:75092200-75095400	Weak transcription	Stomach Smooth Muscle	stomach
50	chr11:75092200-75095400	Weak transcription	Hela-S3	cervix

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