Variant report

Variant	rs192161463
Chromosome Location	chr19:39987304-39987305
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:39947157-39987373	PANC-1	pancreas:	n/a	n/a

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:39925200..39927476-chr19:39987141..39989306,2	K562	blood:
2	chr19:39986104..39989101-chr19:39992054..39994014,2	K562	blood:
3	chr19:39970388..39973416-chr19:39987093..39991960,6	MCF-7	breast:
4	chr19:39987217..39989716-chr19:40005337..40006880,2	MCF-7	breast:
5	chr19:39982701..39986911-chr19:39987055..39990908,4	MCF-7	breast:
6	chr19:39973981..39976601-chr19:39986100..39988186,2	MCF-7	breast:
7	chr19:39925162..39927908-chr19:39986730..39988641,3	K562	blood:
8	chr19:39978061..39981122-chr19:39987269..39990771,3	MCF-7	breast:

No data

Variant related genes	Relation type
DLL3	TF binding region
ENSG00000105193	Chromatin interaction
ENSG00000105197	Chromatin interaction
ENSG00000186838	Chromatin interaction
ENSG00000196235	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv911689	chr19:39903088-40021759	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	nsv911690	chr19:39903088-40046863	Weak transcription Bivalent Enhancer Strong transcription Enhancers Genic enhancers Flanking Active TSS 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	88 gene(s)	inside rSNPs	diseases
3	nsv523856	chr19:39913558-39997472	Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
4	nsv911691	chr19:39979966-40029386	Strong transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv911692	chr19:39979966-40046863	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv1060251	chr19:39982988-40099773	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
7	nsv911693	chr19:39986241-40033574	Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39972800-39988600	Weak transcription	Right Atrium	heart
2	chr19:39973600-39988400	Weak transcription	Fetal Brain Male	brain
3	chr19:39980000-39988600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr19:39980600-39988600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr19:39980800-39988200	Weak transcription	HUVEC	blood vessel
6	chr19:39980800-39988400	Weak transcription	K562	blood
7	chr19:39981000-39988200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr19:39981000-39988400	Weak transcription	Aorta	Aorta
9	chr19:39981000-39988400	Weak transcription	GM12878-XiMat	blood
10	chr19:39981000-39988400	Weak transcription	HSMMtube	muscle
11	chr19:39981000-39988600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr19:39981000-39988600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr19:39981000-39988600	Weak transcription	Gastric	stomach
14	chr19:39981000-39988800	Weak transcription	Pancreas	Pancrea
15	chr19:39981200-39988400	Weak transcription	Primary B cells from peripheral blood	blood
16	chr19:39981400-39988200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr19:39981400-39988400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr19:39981400-39988600	Weak transcription	Primary B cells from cord blood	blood
19	chr19:39981400-39988600	Weak transcription	HSMM	muscle
20	chr19:39981600-39988400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr19:39982800-39987600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr19:39983000-39987600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr19:39983200-39988000	Weak transcription	Liver	Liver
24	chr19:39983200-39988400	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr19:39983200-39988400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr19:39983200-39988400	Weak transcription	Fetal Brain Female	brain
27	chr19:39983200-39988400	Weak transcription	Spleen	Spleen
28	chr19:39983200-39988600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr19:39983200-39988800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr19:39983400-39987600	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr19:39983400-39988200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr19:39983800-39988000	Weak transcription	Brain Germinal Matrix	brain
33	chr19:39983800-39988200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr19:39983800-39988200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr19:39984000-39988200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr19:39984000-39988200	Weak transcription	A549	lung
37	chr19:39984000-39988600	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr19:39984200-39988600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr19:39987000-39987400	Enhancers	HMEC	breast
40	chr19:39987200-39987400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr19:39987200-39988200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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