Variant report

Variant	rs7605576
Chromosome Location	chr2:38767586-38767587
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr2:38767108-38769339	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:38767539-38767594	HepG2	liver:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr2:38766012..38769150-chr2:38977122..38980582,4	K562	blood:
2	chr2:38742072..38744914-chr2:38766653..38769930,3	K562	blood:
3	chr2:38762206..38765447-chr2:38765522..38767637,3	K562	blood:
4	chr2:38756770..38758760-chr2:38767027..38769567,2	K562	blood:
5	chr2:38767365..38769438-chr2:38773461..38775183,2	MCF-7	breast:
6	chr2:38766439..38768320-chr2:38948180..38949983,2	K562	blood:
7	chr2:38751052..38753238-chr2:38767165..38769647,2	MCF-7	breast:
8	chr2:38765872..38769105-chr2:38828205..38830691,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRPLL-1	chr2:38767123-38768717	XLOC_002054

No data

Variant related genes	Relation type
ENSG00000271443	TF binding region
ENSG00000271443	Chromatin interaction
ENSG00000231367	Chromatin interaction
ENSG00000235586	Chromatin interaction
ENSG00000143889	Chromatin interaction
ENSG00000152147	Chromatin interaction
ENSG00000115875	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11894300	1.00[AMR][1000 genomes]
rs12105066	1.00[AMR][1000 genomes]
rs17023010	1.00[AMR][1000 genomes]
rs57091543	1.00[AMR][1000 genomes]
rs58185217	0.90[AFR][1000 genomes]
rs59492432	1.00[AMR][1000 genomes]
rs61048190	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73929028	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73929071	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73929074	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73929083	1.00[AMR][1000 genomes]
rs73929101	1.00[AMR][1000 genomes]
rs73931607	1.00[AMR][1000 genomes]
rs7591739	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916059	chr2:38332341-39119398	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	143 gene(s)	inside rSNPs	diseases
2	nsv9646	chr2:38358311-39082189	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
3	nsv873881	chr2:38745624-38877636	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	esv1796304	chr2:38766721-38790750	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:38763400-38768000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:38763600-38767600	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr2:38763600-38767800	Weak transcription	Stomach Mucosa	stomach
4	chr2:38763600-38768200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr2:38763600-38768200	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr2:38763600-38768400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:38763600-38768800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr2:38763600-38769000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr2:38763600-38770200	Weak transcription	HSMMtube	muscle
10	chr2:38763600-38771000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr2:38763600-38809600	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr2:38763800-38767600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr2:38763800-38767600	Weak transcription	Colon Smooth Muscle	Colon
14	chr2:38763800-38767600	Weak transcription	Fetal Brain Male	brain
15	chr2:38763800-38767600	Weak transcription	Fetal Intestine Large	intestine
16	chr2:38763800-38767600	Weak transcription	Fetal Intestine Small	intestine
17	chr2:38763800-38767600	Weak transcription	Rectal Smooth Muscle	rectum
18	chr2:38763800-38767800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr2:38763800-38767800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr2:38763800-38767800	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr2:38763800-38768400	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr2:38763800-38768600	Weak transcription	Brain Anterior Caudate	brain
23	chr2:38763800-38769000	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr2:38763800-38769400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr2:38763800-38769800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr2:38763800-38778800	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr2:38764200-38768400	Weak transcription	Liver	Liver
28	chr2:38764200-38769600	Weak transcription	A549	lung
29	chr2:38765600-38768200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr2:38765600-38768400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr2:38765800-38768000	Enhancers	HepG2	liver
32	chr2:38766600-38767600	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr2:38766600-38768200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr2:38766600-38768200	Weak transcription	Duodenum Mucosa	Duodenum
35	chr2:38766800-38768200	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr2:38767200-38769400	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr2:38767400-38768400	Enhancers	Fetal Brain Female	brain
38	chr2:38767400-38768400	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr2:38767400-38768600	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr2:38767400-38768800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr2:38767400-38770000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr2:38767400-38773400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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