Variant report

Variant	rs577568068
Chromosome Location	chr14:38052687-38052688
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:114300280..114302664-chr14:38052543..38054233,2	MCF-7	breast:
2	chr14:38035593..38036192-chr14:38052628..38053371,2	MCF-7	breast:
3	chr14:38052050..38054072-chr8:119123824..119125742,2	MCF-7	breast:
4	chr14:38052164..38054489-chr14:38155614..38158177,2	MCF-7	breast:
5	chr14:38021477..38023434-chr14:38051873..38053665,2	MCF-7	breast:
6	chr14:38013794..38017816-chr14:38049871..38055560,6	MCF-7	breast:
7	chr14:37697487..37699947-chr14:38052550..38054920,2	MCF-7	breast:
8	chr14:38051959..38054896-chr14:38346073..38349054,2	MCF-7	breast:
9	chr11:62607623..62609133-chr14:38052681..38055666,2	MCF-7	breast:
10	chr14:38052576..38054584-chr20:45987058..45989218,2	MCF-7	breast:
11	chr14:38050621..38053581-chr14:38135495..38137848,2	MCF-7	breast:
12	chr14:37709149..37730989-chr14:38048141..38067789,135	MCF-7	breast:
13	chr14:37747627..37749985-chr14:38051291..38052830,2	MCF-7	breast:
14	chr14:38010426..38020494-chr14:38050537..38062032,33	MCF-7	breast:
15	chr14:37697471..37699396-chr14:38051501..38053443,2	MCF-7	breast:
16	chr14:37708906..37733371-chr14:38048131..38068843,170	MCF-7	breast:
17	chr14:38052525..38053293-chr14:38064796..38065530,4	MCF-7	breast:
18	chr14:38051074..38053594-chr16:89788190..89790581,2	MCF-7	breast:
19	chr14:38052352..38053048-chr14:38063149..38064449,4	MCF-7	breast:
20	chr14:38052525..38053293-chr14:38064796..38065530,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000116793	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000158805	Chromatin interaction
ENSG00000129514	Chromatin interaction
ENSG00000151338	Chromatin interaction
ENSG00000182197	Chromatin interaction
ENSG00000139865	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530038	chr14:37590543-38336191	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv826923	chr14:38017619-38108645	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
3	nsv832772	chr14:38030300-38225921	Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
4	nsv901642	chr14:38041870-38081005	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
5	nsv901643	chr14:38047789-38081005	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
6	nsv901644	chr14:38049107-38064738	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
7	nsv901645	chr14:38051035-38064215	Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
8	nsv901646	chr14:38051035-38081005	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
9	nsv901647	chr14:38052110-38064738	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
10	nsv901648	chr14:38052110-38065813	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
11	nsv916985	chr14:38052347-38838551	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38051800-38053600	Active TSS	HepG2	liver
2	chr14:38051800-38054600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
3	chr14:38052000-38055200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
4	chr14:38052200-38053400	Active TSS	A549	lung
5	chr14:38052200-38053800	Active TSS	Rectal Mucosa Donor 29	rectum
6	chr14:38052200-38054200	Bivalent/Poised TSS	Fetal Intestine Small	intestine
7	chr14:38052400-38052800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr14:38052400-38052800	Bivalent Enhancer	NH-A	brain
9	chr14:38052400-38053000	Bivalent/Poised TSS	Stomach Mucosa	stomach
10	chr14:38052400-38053200	Bivalent/Poised TSS	Lung	lung
11	chr14:38052400-38053400	Bivalent/Poised TSS	Fetal Intestine Large	intestine
12	chr14:38052400-38053400	Bivalent/Poised TSS	Small Intestine	intestine
13	chr14:38052400-38053400	Active TSS	Hela-S3	cervix
14	chr14:38052400-38053600	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr14:38052400-38053600	Active TSS	Rectal Mucosa Donor 31	rectum
16	chr14:38052400-38054600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr14:38052400-38054800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
18	chr14:38052400-38054800	Active TSS	Esophagus	oesophagus
19	chr14:38052600-38052800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr14:38052600-38052800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
21	chr14:38052600-38052800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
22	chr14:38052600-38052800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr14:38052600-38052800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr14:38052600-38052800	Bivalent/Poised TSS	Brain Anterior Caudate	brain
25	chr14:38052600-38052800	Bivalent Enhancer	Brain Germinal Matrix	brain
26	chr14:38052600-38052800	Bivalent Enhancer	Psoas Muscle	Psoas
27	chr14:38052600-38052800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
28	chr14:38052600-38053000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
29	chr14:38052600-38053000	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr14:38052600-38053000	Bivalent Enhancer	Adipose Nuclei	Adipose
31	chr14:38052600-38053000	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
32	chr14:38052600-38053000	Bivalent/Poised TSS	Fetal Stomach	stomach
33	chr14:38052600-38053000	Active TSS	Gastric	stomach
34	chr14:38052600-38053200	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr14:38052600-38053200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr14:38052600-38053200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
37	chr14:38052600-38053200	Active TSS	Liver	Liver
38	chr14:38052600-38053200	Bivalent Enhancer	Placenta	Placenta
39	chr14:38052600-38053200	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
40	chr14:38052600-38053400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
41	chr14:38052600-38053400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr14:38052600-38053400	Bivalent/Poised TSS	Colonic Mucosa	Colon
43	chr14:38052600-38053600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr14:38052600-38053600	Enhancers	Pancreas	Pancrea
45	chr14:38052600-38053800	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr14:38052600-38053800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr14:38052600-38053800	Bivalent Enhancer	Fetal Heart	heart
48	chr14:38052600-38053800	Active TSS	Rectal Smooth Muscle	rectum
49	chr14:38052600-38054200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
50	chr14:38052600-38054200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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