Variant report

Variant	rs10416091
Chromosome Location	chr19:44023778-44023779
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr19:43950463..43951811-chr19:44023286..44024411,8	MCF-7	breast:
2	chr19:43950829..43952315-chr19:44023277..44024591,13	MCF-7	breast:
3	chr19:43950879..43951915-chr19:44023292..44024529,15	K562	blood:
4	chr19:43967611..43968675-chr19:44023287..44024342,3	K562	blood:
5	chr19:43936817..43937670-chr19:44023393..44024322,3	K562	blood:
6	chr19:44007109..44009173-chr19:44021498..44024466,3	MCF-7	breast:
7	chr19:43967016..43970562-chr19:44022266..44025437,4	MCF-7	breast:
8	chr19:43936775..43937531-chr19:44023386..44024282,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000176531	Chromatin interaction
ENSG00000124466	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10405049	1.00[AFR][1000 genomes]
rs10405847	1.00[YRI][hapmap]
rs10409032	1.00[ASW][hapmap]
rs3213238	1.00[YRI][hapmap]
rs3213304	1.00[ASW][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055872	chr19:43173614-44075193	Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv544009	chr19:43173614-44075193	Enhancers ZNF genes & repeats Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv1067126	chr19:43260649-44075194	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv544015	chr19:43260649-44075194	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
5	nsv1057657	chr19:43302497-44076564	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
6	nsv1059631	chr19:43316978-44075054	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
7	nsv544030	chr19:43316978-44075054	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
8	nsv532820	chr19:43807486-44080610	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
9	nsv1056721	chr19:43808474-44095077	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
10	nsv532821	chr19:43842383-44357315	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
11	nsv1058162	chr19:43846238-44055058	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
12	nsv1056785	chr19:44010370-44081601	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:44009200-44029200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr19:44009200-44029600	Weak transcription	Psoas Muscle	Psoas
3	chr19:44011200-44029400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr19:44013000-44028600	Weak transcription	Colon Smooth Muscle	Colon
5	chr19:44013000-44028800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr19:44013200-44028600	Weak transcription	Brain Hippocampus Middle	brain
7	chr19:44013200-44029800	Weak transcription	Small Intestine	intestine
8	chr19:44013400-44023800	Weak transcription	Fetal Lung	lung
9	chr19:44013400-44029400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr19:44014400-44029400	Weak transcription	Dnd41	blood
11	chr19:44015200-44028600	Weak transcription	Primary hematopoietic stem cells	blood
12	chr19:44015200-44028800	Weak transcription	Gastric	stomach
13	chr19:44015400-44028400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr19:44015400-44028800	Weak transcription	Fetal Thymus	thymus
15	chr19:44015400-44028800	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr19:44015400-44029000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr19:44015400-44029200	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr19:44015400-44029400	Weak transcription	Brain Germinal Matrix	brain
19	chr19:44015400-44029600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr19:44015600-44027000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr19:44015600-44027000	Weak transcription	A549	lung
22	chr19:44015600-44028400	Weak transcription	Stomach Smooth Muscle	stomach
23	chr19:44015600-44028600	Weak transcription	Adipose Nuclei	Adipose
24	chr19:44015600-44028800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr19:44015600-44028800	Weak transcription	HepG2	liver
26	chr19:44015600-44029400	Weak transcription	Brain Anterior Caudate	brain
27	chr19:44015600-44029600	Weak transcription	Brain Substantia Nigra	brain
28	chr19:44015800-44025200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr19:44015800-44025200	Weak transcription	HMEC	breast
30	chr19:44015800-44028800	Weak transcription	Fetal Intestine Large	intestine
31	chr19:44015800-44028800	Weak transcription	Rectal Smooth Muscle	rectum
32	chr19:44015800-44029000	Weak transcription	Fetal Muscle Trunk	muscle
33	chr19:44015800-44029000	Weak transcription	Thymus	Thymus
34	chr19:44015800-44029000	Weak transcription	NHDF-Ad	bronchial
35	chr19:44015800-44029000	Weak transcription	NHLF	lung
36	chr19:44015800-44029200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr19:44015800-44029400	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr19:44015800-44029400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr19:44015800-44029400	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr19:44015800-44029400	Weak transcription	Brain Angular Gyrus	brain
41	chr19:44015800-44029400	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr19:44015800-44029400	Weak transcription	Fetal Brain Female	brain
43	chr19:44015800-44029400	Weak transcription	Left Ventricle	heart
44	chr19:44015800-44029800	Weak transcription	Aorta	Aorta
45	chr19:44015800-44030000	Weak transcription	Ovary	ovary
46	chr19:44017000-44027000	Strong transcription	Fetal Intestine Small	intestine
47	chr19:44017200-44028800	Weak transcription	Spleen	Spleen
48	chr19:44017400-44028800	Weak transcription	Esophagus	oesophagus
49	chr19:44017600-44026800	Weak transcription	Colonic Mucosa	Colon
50	chr19:44017600-44027200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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