Variant report

Variant	rs74029146
Chromosome Location	chr15:93152721-93152722
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:93138971..93141696-chr15:93151230..93154019,2	MCF-7	breast:
2	chr15:93145822..93150486-chr15:93150497..93155016,6	K562	blood:
3	chr15:93151753..93155694-chr15:93155809..93157941,4	MCF-7	breast:
4	chr15:93150012..93154507-chr15:93196255..93200347,4	MCF-7	breast:
5	chr15:93146362..93148233-chr15:93152029..93154921,2	K562	blood:

Variant related genes	Relation type
ENSG00000260337	Chromatin interaction
ENSG00000185442	Chromatin interaction
ENSG00000271763	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs16947074	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16947087	1.00[EUR][1000 genomes]
rs28607954	1.00[EUR][1000 genomes]
rs56356816	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56411549	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60198063	1.00[EUR][1000 genomes]
rs60202325	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60773454	1.00[EUR][1000 genomes]
rs61648904	1.00[EUR][1000 genomes]
rs7162641	1.00[ASN][1000 genomes]
rs7169192	1.00[ASN][1000 genomes]
rs73452882	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73452888	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73454733	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73531783	1.00[EUR][1000 genomes]
rs74029102	1.00[EUR][1000 genomes]
rs74029103	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74029116	1.00[EUR][1000 genomes]
rs74029127	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74029128	1.00[EUR][1000 genomes]
rs74029129	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74029130	1.00[EUR][1000 genomes]
rs74029131	1.00[EUR][1000 genomes]
rs74029132	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74029133	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74029134	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74029135	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74029136	1.00[EUR][1000 genomes]
rs74029137	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74029141	1.00[EUR][1000 genomes]
rs74029147	1.00[EUR][1000 genomes]
rs74029148	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74029149	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74029150	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74029153	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74031608	1.00[EUR][1000 genomes]
rs74031611	1.00[EUR][1000 genomes]
rs74031613	1.00[EUR][1000 genomes]
rs74031614	1.00[EUR][1000 genomes]
rs74031617	1.00[EUR][1000 genomes]
rs74031618	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948621	chr15:92688981-93158095	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1037972	chr15:92804908-93270761	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
3	nsv904499	chr15:92914795-93472582	Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	163 gene(s)	inside rSNPs	diseases
4	nsv948738	chr15:93070742-93728147	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
5	nsv1049490	chr15:93134405-93591660	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	151 gene(s)	inside rSNPs	diseases
6	esv1808537	chr15:93146057-93191935	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:93139400-93159800	Weak transcription	Fetal Lung	lung
2	chr15:93142200-93156400	Weak transcription	Lung	lung
3	chr15:93142200-93160400	Weak transcription	Right Atrium	heart
4	chr15:93143600-93160000	Weak transcription	Right Ventricle	heart
5	chr15:93146800-93160000	Weak transcription	Psoas Muscle	Psoas
6	chr15:93150000-93153200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:93150000-93153200	Weak transcription	Fetal Muscle Leg	muscle
8	chr15:93150000-93153600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr15:93150000-93155600	Weak transcription	Pancreas	Pancrea
10	chr15:93150000-93160600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr15:93150200-93157000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr15:93150400-93156200	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr15:93150400-93156400	Weak transcription	Fetal Stomach	stomach
14	chr15:93151200-93157200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr15:93151200-93160200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr15:93151400-93157600	Weak transcription	Fetal Intestine Small	intestine
17	chr15:93151400-93167400	Weak transcription	Brain Germinal Matrix	brain
18	chr15:93151600-93152800	Weak transcription	Gastric	stomach
19	chr15:93151600-93158600	Weak transcription	HSMMtube	muscle
20	chr15:93151600-93159600	Weak transcription	HSMM	muscle
21	chr15:93151600-93178000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr15:93151800-93155600	Weak transcription	Stomach Smooth Muscle	stomach
23	chr15:93152200-93153000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr15:93152200-93153000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr15:93152400-93152800	Enhancers	Esophagus	oesophagus
26	chr15:93152400-93152800	Enhancers	Stomach Mucosa	stomach
27	chr15:93152600-93158000	Weak transcription	Fetal Muscle Trunk	muscle

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