Variant report

Variant	rs74033755
Chromosome Location	chr15:100222670-100222671
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr15:100222668-100223023	IMR90	lung:	n/a	chr15:100222824-100222836
2	MYC	chr15:100222666-100222881	MCF10A-Er-Src	breast:	n/a	chr15:100222838-100222847
3	JUND	chr15:100222611-100222985	K562	blood:	n/a	n/a
4	NFIC	chr15:100222474-100223105	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:100220233..100222565-chr15:100222577..100224923,2	MCF-7	breast:
2	chr15:100104936..100107605-chr15:100221549..100224496,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000201724	TF binding region
ENSG00000201724	Chromatin interaction
ENSG00000068305	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs74033746	1.00[AMR][1000 genomes]
rs74033747	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036346	chr15:99752391-100365458	Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv542520	chr15:99752391-100365458	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv817201	chr15:99839238-100537341	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	nsv1038005	chr15:100170414-100633714	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	nsv542522	chr15:100170414-100633714	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
6	nsv904559	chr15:100174907-100255046	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	nsv904560	chr15:100196657-100339331	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	nsv904561	chr15:100204918-100486828	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers 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	20 gene(s)	inside rSNPs	diseases
9	nsv904562	chr15:100214935-100237682	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:100159000-100253000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:100171200-100232800	Weak transcription	Esophagus	oesophagus
3	chr15:100171200-100248800	Weak transcription	Gastric	stomach
4	chr15:100172000-100230800	Weak transcription	Stomach Mucosa	stomach
5	chr15:100179200-100232600	Weak transcription	Colonic Mucosa	Colon
6	chr15:100181800-100232800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr15:100192000-100230400	Weak transcription	NHLF	lung
8	chr15:100193000-100229000	Weak transcription	Lung	lung
9	chr15:100199800-100232600	Weak transcription	Right Ventricle	heart
10	chr15:100209800-100224400	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr15:100209800-100232800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr15:100210800-100223400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:100211800-100232200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr15:100212800-100223800	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr15:100212800-100240000	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr15:100213000-100232600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr15:100213200-100250800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr15:100213400-100226400	Weak transcription	Fetal Brain Male	brain
19	chr15:100213400-100232600	Weak transcription	Pancreas	Pancrea
20	chr15:100213600-100243400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr15:100214400-100223200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr15:100214400-100223400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr15:100214400-100224200	Strong transcription	Rectal Mucosa Donor 31	rectum
24	chr15:100215000-100224600	Strong transcription	Liver	Liver
25	chr15:100215600-100226400	Weak transcription	HepG2	liver
26	chr15:100215800-100223000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr15:100215800-100223400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr15:100215800-100230800	Weak transcription	Stomach Smooth Muscle	stomach
29	chr15:100216000-100222800	Weak transcription	Brain Cingulate Gyrus	brain
30	chr15:100216000-100223800	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr15:100216000-100224600	Weak transcription	Brain Germinal Matrix	brain
32	chr15:100216000-100224600	Weak transcription	Brain Substantia Nigra	brain
33	chr15:100216200-100222800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr15:100216200-100226400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr15:100216200-100229800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr15:100216200-100230200	Weak transcription	HMEC	breast
37	chr15:100216200-100232600	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr15:100216200-100233000	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr15:100216400-100229600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr15:100216800-100222800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr15:100216800-100230200	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr15:100216800-100230400	Weak transcription	Placenta	Placenta
43	chr15:100216800-100232200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr15:100217000-100232800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr15:100217200-100227200	Weak transcription	Fetal Stomach	stomach
46	chr15:100217400-100232600	Weak transcription	Fetal Intestine Small	intestine
47	chr15:100218000-100223200	Weak transcription	Fetal Muscle Leg	muscle
48	chr15:100218000-100230400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr15:100218200-100226200	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr15:100218200-100232600	Weak transcription	Hela-S3	cervix

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