Variant report

Variant	rs115685555
Chromosome Location	chr19:56631768-56631769
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	chr19:56631390..56634909-chr19:56825062..56827444,3	MCF-7	breast:
2	chr19:56629557..56632352-chr19:56654228..56656025,2	K562	blood:
3	chr19:56630391..56632820-chr19:56902199..56906311,3	K562	blood:
4	chr19:56629872..56632038-chr19:56819906..56821500,2	MCF-7	breast:
5	chr19:56629808..56631953-chr19:56643126..56645330,2	K562	blood:
6	chr19:56630500..56632010-chr19:56658354..56660515,2	MCF-7	breast:
7	chr19:56631391..56633030-chr19:56824712..56827583,2	K562	blood:
8	chr19:56627257..56634581-chr19:56650310..56656612,28	MCF-7	breast:
9	chr14:90422308..90422816-chr19:56631324..56632109,2	Hela-S3	cervix:
10	chr19:56629593..56636020-chr19:56650029..56654099,17	K562	blood:
11	chr19:56629946..56632652-chr19:56657182..56659175,2	K562	blood:
12	chr19:56630318..56632496-chr21:46494292..46496510,2	K562	blood:
13	chr19:56630391..56632820-chr19:56902199..56904998,2	K562	blood:
14	chr19:55626838..55628634-chr19:56630662..56632626,2	MCF-7	breast:
15	chr19:56631659..56633594-chr19:56825559..56827609,3	MCF-7	breast:
16	chr19:56631557..56632388-chr22:32145652..32146286,2	Hela-S3	cervix:
17	chr19:56629593..56635165-chr19:56650391..56656450,20	K562	blood:
18	chr19:56165463..56168899-chr19:56631045..56633379,3	K562	blood:
19	chr19:56605498..56607205-chr19:56630684..56632400,2	K562	blood:
20	chr19:56629015..56635457-chr19:56649954..56657591,25	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000125503	Chromatin interaction
ENSG00000267454	Chromatin interaction
ENSG00000183530	Chromatin interaction
ENSG00000197381	Chromatin interaction
ENSG00000063244	Chromatin interaction
ENSG00000167685	Chromatin interaction
ENSG00000267549	Chromatin interaction
ENSG00000018869	Chromatin interaction
ENSG00000042088	Chromatin interaction
ENSG00000131848	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1056598	chr19:56331762-56703428	Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
2	nsv1064371	chr19:56418215-56842450	ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
3	nsv1057316	chr19:56418215-56849458	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
4	nsv580354	chr19:56505685-56723492	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
5	nsv833883	chr19:56512601-56640089	Strong transcription Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
6	nsv523651	chr19:56537528-56707048	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
7	nsv1057820	chr19:56555942-56720262	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
8	nsv528998	chr19:56578238-56707048	Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
9	nsv912512	chr19:56592286-56636759	Enhancers Genic enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
10	nsv517365	chr19:56592286-56674548	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
11	nsv912513	chr19:56592286-56685463	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
12	nsv521744	chr19:56592286-56686953	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
13	nsv912514	chr19:56596815-56636759	Flanking Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
14	nsv912516	chr19:56601298-56981382	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	93 gene(s)	inside rSNPs	diseases
15	esv1809307	chr19:56604027-56633623	Enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
16	esv1824038	chr19:56610449-56636632	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
17	esv3331653	chr19:56631165-56634013	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	n/a
18	esv3409452	chr19:56631390-56633688	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56624200-56631800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr19:56629400-56631800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr19:56630000-56631800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
4	chr19:56630000-56631800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr19:56630200-56631800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr19:56630400-56631800	Flanking Active TSS	Colonic Mucosa	Colon
7	chr19:56630400-56631800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
8	chr19:56630400-56632000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr19:56630400-56632000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr19:56630400-56632000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
11	chr19:56630800-56631800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr19:56630800-56631800	Flanking Active TSS	Stomach Mucosa	stomach
13	chr19:56630800-56631800	Flanking Active TSS	NHLF	lung
14	chr19:56631000-56631800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr19:56631000-56631800	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr19:56631000-56631800	Flanking Active TSS	Primary hematopoietic stem cells	blood
17	chr19:56631000-56631800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr19:56631000-56631800	Flanking Active TSS	Fetal Muscle Trunk	muscle
19	chr19:56631000-56631800	Flanking Active TSS	Fetal Muscle Leg	muscle
20	chr19:56631000-56632000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
21	chr19:56631000-56632000	Flanking Active TSS	Placenta	Placenta
22	chr19:56631000-56632000	Flanking Active TSS	Dnd41	blood
23	chr19:56631000-56632200	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr19:56631000-56632600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
25	chr19:56631000-56633200	Active TSS	H9 Cell Line	embryonic stem cell
26	chr19:56631000-56633200	Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr19:56631000-56633400	Active TSS	Small Intestine	intestine
28	chr19:56631000-56633600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr19:56631200-56631800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr19:56631200-56631800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr19:56631200-56631800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
32	chr19:56631200-56631800	Flanking Active TSS	Stomach Smooth Muscle	stomach
33	chr19:56631200-56632000	Flanking Active TSS	Primary B cells from cord blood	blood
34	chr19:56631200-56632000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
35	chr19:56631200-56632000	Flanking Active TSS	Fetal Brain Male	brain
36	chr19:56631200-56632000	Flanking Active TSS	Fetal Brain Female	brain
37	chr19:56631200-56632000	Active TSS	Fetal Kidney	kidney
38	chr19:56631200-56632000	Flanking Active TSS	Fetal Thymus	thymus
39	chr19:56631200-56632200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
40	chr19:56631200-56632800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr19:56631200-56633400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr19:56631200-56633600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr19:56631200-56633600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr19:56631200-56633600	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr19:56631200-56633800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr19:56631400-56631800	Flanking Active TSS	Brain Germinal Matrix	brain
47	chr19:56631400-56632000	Flanking Active TSS	Primary B cells from peripheral blood	blood
48	chr19:56631400-56632000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
49	chr19:56631400-56632000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
50	chr19:56631400-56633200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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