Variant report

Variant	rs7671320
Chromosome Location	chr4:8601381-8601382
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:14)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:14 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MYC	chr4:8601343-8601713	MCF10A-Er-Src	breast:	n/a	n/a
2	MAX	chr4:8601369-8601754	NB4	blood:	n/a	n/a
3	MXI1	chr4:8601141-8601794	IMR90	lung:	n/a	n/a
4	JUND	chr4:8601226-8601867	HCT-116	colon:	n/a	n/a
5	FOSL1	chr4:8601360-8601755	K562	blood:	n/a	chr4:8601574-8601585
6	NFIC	chr4:8601240-8601835	ECC-1	luminal epithelium:	n/a	n/a
7	FOSL1	chr4:8601254-8601879	HCT-116	colon:	n/a	chr4:8601574-8601585
8	NFIC	chr4:8601275-8601825	ECC-1	luminal epithelium:	n/a	n/a
9	MAX	chr4:8601339-8601693	ECC-1	luminal epithelium:	n/a	n/a
10	RCOR1	chr4:8601321-8601759	K562	blood:	n/a	n/a
11	JUND	chr4:8601376-8601792	K562	blood:	n/a	n/a
12	FOSL1	chr4:8601284-8601870	HCT-116	colon:	n/a	chr4:8601574-8601585
13	JUN	chr4:8601026-8601824	K562	blood:	n/a	n/a
14	MAZ	chr4:8601242-8602052	IMR90	lung:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:8595691..8598338-chr4:8600228..8602977,2	MCF-7	breast:
2	chr4:8600582..8603192-chr4:8603240..8605634,2	K562	blood:
3	chr4:8595995..8599950-chr4:8600230..8602284,3	K562	blood:
4	chr4:8596740..8598589-chr4:8600076..8602284,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-METTL19-6	chr4:8601180-8601688	NONHSAT095111

No data

Variant related genes	Relation type
GPR78	TF binding region
CPZ	TF binding region
ENSG00000109625	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10938726	0.89[EUR][1000 genomes]
rs2241069	0.83[ASN][1000 genomes]
rs34964084	0.82[EUR][1000 genomes]
rs3756168	0.81[EUR][1000 genomes]
rs3756171	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3822205	0.81[EUR][1000 genomes]
rs4696699	0.82[EUR][1000 genomes]
rs4696702	0.82[EUR][1000 genomes]
rs7663886	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7677259	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv878604	chr4:8315938-8618916	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh 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
2	nsv1002680	chr4:8357163-8721214	Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv878612	chr4:8534283-8618916	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv1832730	chr4:8541086-9514568	Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
5	esv1843578	chr4:8541086-9514568	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
6	nsv878613	chr4:8554894-8618916	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv878614	chr4:8554894-8669619	Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv878615	chr4:8566758-8625245	Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv878616	chr4:8566758-8669619	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv878617	chr4:8566758-9371116	ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
11	nsv1014219	chr4:8578779-8724531	Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
12	nsv878618	chr4:8579758-8641696	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
13	nsv878619	chr4:8579758-8669619	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
14	nsv878620	chr4:8584879-8674871	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
15	nsv470015	chr4:8584879-8729638	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
16	nsv878621	chr4:8584879-9371116	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
17	nsv878622	chr4:8599250-9371116	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8573400-8609400	Weak transcription	Right Atrium	heart
2	chr4:8596000-8622800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:8596000-8623200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr4:8596200-8601400	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr4:8596200-8601400	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr4:8596200-8602000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr4:8596200-8609000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr4:8596400-8602000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr4:8596400-8602000	Weak transcription	NHLF	lung
10	chr4:8597400-8604400	Weak transcription	Fetal Intestine Small	intestine
11	chr4:8597600-8618400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr4:8598400-8601600	Genic enhancers	Ovary	ovary
13	chr4:8598800-8609000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr4:8599400-8602200	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr4:8599600-8616000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr4:8599800-8609000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr4:8600200-8603200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr4:8600600-8601800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr4:8600600-8602000	Enhancers	HSMM	muscle
20	chr4:8600600-8603000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr4:8600600-8605800	Strong transcription	Placenta Amnion	Placenta Amnion
22	chr4:8600800-8601600	Enhancers	NHDF-Ad	bronchial
23	chr4:8600800-8601800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr4:8600800-8601800	Enhancers	NH-A	brain
25	chr4:8600800-8602200	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
26	chr4:8600800-8603200	Bivalent Enhancer	Fetal Muscle Leg	muscle
27	chr4:8600800-8603200	Strong transcription	Placenta	Placenta
28	chr4:8600800-8608400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
29	chr4:8601000-8601400	Enhancers	HSMMtube	muscle
30	chr4:8601000-8601800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr4:8601000-8601800	Enhancers	Osteobl	bone
32	chr4:8601200-8601600	Enhancers	A549	lung
33	chr4:8601200-8601800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr4:8601200-8601800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr4:8601200-8601800	Enhancers	Hela-S3	cervix
36	chr4:8601200-8602400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
37	chr4:8601200-8611400	Weak transcription	Spleen	Spleen

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