Variant report

Variant	rs10471184
Chromosome Location	chr4:187122904-187122905
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:33)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:33 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	E2F6	chr4:187122650-187123364	H1-hESC	embryonic stem cell:	n/a	n/a
2	MAX	chr4:187122870-187123400	A549	lung:	n/a	n/a
3	MYC	chr4:187122856-187123285	A549	lung:	n/a	n/a
4	RAD21	chr4:187122890-187123479	HCT-116	colon:	n/a	n/a
5	STAT3	chr4:187122800-187122980	MCF10A-Er-Src	breast:	n/a	n/a
6	POLR2A	chr4:187122824-187123286	MCF10A-Er-Src	breast:	n/a	n/a
7	MAX	chr4:187122865-187123450	HepG2	liver:	n/a	n/a
8	MXI1	chr4:187122820-187123314	H1-hESC	embryonic stem cell:	n/a	n/a
9	RAD21	chr4:187122901-187123337	A549	lung:	n/a	n/a
10	SPI1	chr4:187122653-187123033	HL-60	blood:	n/a	n/a
11	CTCF	chr4:187122841-187123478	MCF-7	breast:	n/a	n/a
12	MAX	chr4:187122726-187123382	NB4	blood:	n/a	n/a
13	POLR2A	chr4:187122831-187123362	Hela-S3	cervix:	n/a	n/a
14	MAX	chr4:187122866-187123493	MCF-7	breast:	n/a	n/a
15	CTCF	chr4:187122598-187123620	HCT-116	colon:	n/a	n/a
16	CTCF	chr4:187122893-187123341	HepG2	liver:	n/a	n/a
17	CTCF	chr4:187122697-187123571	A549	lung:	n/a	n/a
18	RAD21	chr4:187122894-187123356	H1-hESC	embryonic stem cell:	n/a	n/a
19	GTF2F1	chr4:187122852-187123275	H1-hESC	embryonic stem cell:	n/a	n/a
20	MAX	chr4:187122744-187123350	H1-hESC	embryonic stem cell:	n/a	n/a
21	SPI1	chr4:187122726-187122922	GM12891	blood:	n/a	n/a
22	MYC	chr4:187122734-187123346	H1-hESC	embryonic stem cell:	n/a	n/a
23	MAX	chr4:187122662-187123500	HCT-116	colon:	n/a	n/a
24	USF1	chr4:187122861-187123437	HCT-116	colon:	n/a	n/a
25	RAD21	chr4:187122786-187123514	HCT-116	colon:	n/a	n/a
26	MAX	chr4:187122593-187123503	HCT-116	colon:	n/a	n/a
27	CTCF	chr4:187122847-187123487	HCT-116	colon:	n/a	n/a
28	EGR1	chr4:187122839-187123574	HCT-116	colon:	n/a	chr4:187123162-187123176
29	MAX	chr4:187122641-187123422	H1-hESC	embryonic stem cell:	n/a	n/a
30	MAX	chr4:187122842-187123487	A549	lung:	n/a	n/a
31	CTCF	chr4:187122876-187123411	GM12878	blood:	n/a	n/a
32	CTCF	chr4:187122677-187123566	SK-N-SH	brain:	n/a	n/a
33	MAX	chr4:187122748-187123419	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:187109253..187118277-chr4:187122555..187126883,14	K562	blood:
2	chr4:187111353..187115983-chr4:187119045..187124895,10	MCF-7	breast:
3	chr4:186988972..186989928-chr4:187122701..187123491,2	MCF-7	breast:
4	chr4:187116069..187118838-chr4:187120195..187124189,4	MCF-7	breast:
5	chr4:187058298..187058901-chr4:187122712..187123588,2	MCF-7	breast:
6	chr4:187112006..187113547-chr4:187122764..187123712,6	MCF-7	breast:
7	chr4:187118539..187120138-chr4:187121607..187123644,3	MCF-7	breast:
8	chr4:187121686..187123375-chr4:187456206..187458817,2	K562	blood:
9	chr4:187122087..187123852-chr4:187421026..187423788,3	K562	blood:

No data

Variant related genes	Relation type
CYP4V2	TF binding region
ENSG00000251165	Chromatin interaction
ENSG00000212387	Chromatin interaction
ENSG00000145476	Chromatin interaction
ENSG00000269302	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10025990	0.83[CEU][hapmap]
rs1511800	1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.88[EUR][1000 genomes]
rs1877320	1.00[CEU][hapmap];0.82[JPT][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2102575	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3087505	0.91[CEU][hapmap];0.95[GIH][hapmap];0.88[TSI][hapmap]
rs4862665	1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.88[EUR][1000 genomes]
rs4862666	1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.88[EUR][1000 genomes]
rs4862668	0.83[EUR][1000 genomes]
rs6842047	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72647308	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7697077	0.88[EUR][1000 genomes]
rs9995366	1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];1.00[TSI][hapmap];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:44 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028146	chr4:186503899-187338335	Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv530178	chr4:186659940-187478310	Bivalent Enhancer Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers 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	26 gene(s)	inside rSNPs	diseases
3	nsv931977	chr4:186912987-187364756	Active TSS Strong transcription Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv461860	chr4:186929226-187131504	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv596389	chr4:186929226-187131504	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	nsv1026585	chr4:186929542-187130319	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	nsv537426	chr4:186929542-187130319	Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
8	nsv881037	chr4:186929646-187127817	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
9	nsv461861	chr4:186929646-187129995	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
10	nsv596390	chr4:186929646-187129995	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
11	nsv880709	chr4:186929646-187131384	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
12	nsv880451	chr4:186929646-187148071	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
13	nsv880596	chr4:186931910-187127817	Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
14	nsv880996	chr4:186931910-187131384	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
15	nsv461863	chr4:186931910-187131504	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
16	nsv470097	chr4:186931910-187131504	Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
17	nsv596391	chr4:186931910-187131504	Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
18	nsv1027118	chr4:186935586-187133222	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
19	nsv537427	chr4:186935586-187133222	Active TSS Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
20	nsv1027514	chr4:186935786-187133083	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
21	nsv537428	chr4:186935786-187133083	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
22	nsv1015725	chr4:186936404-187130319	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
23	nsv537429	chr4:186936404-187130319	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
24	nsv881454	chr4:186944884-187131384	Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
25	nsv869299	chr4:186958290-187192748	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
26	nsv880981	chr4:186961015-187148071	Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
27	nsv880485	chr4:186978366-187148071	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
28	nsv1033203	chr4:186990348-187333476	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
29	nsv537431	chr4:186990348-187333476	Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
30	nsv880744	chr4:187004074-187127817	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
31	nsv881579	chr4:187004074-187148071	Strong transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
32	nsv461864	chr4:187006806-187257004	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
33	nsv596392	chr4:187006806-187257004	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS 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
34	nsv830172	chr4:187012765-187168424	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
35	nsv880408	chr4:187021315-187148071	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
36	nsv508340	chr4:187059173-187136958	Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
37	nsv461865	chr4:187072383-187366649	Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
38	nsv596401	chr4:187072383-187366649	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
39	nsv1023019	chr4:187082701-187153933	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
40	nsv1022059	chr4:187082701-187183953	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers 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	13 gene(s)	inside rSNPs	diseases
41	nsv1015923	chr4:187084714-187139572	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
42	nsv537433	chr4:187084714-187139572	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
43	nsv4642	chr4:187085182-187136414	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
44	esv3439419	chr4:187121758-187126356	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs10471184	CYP4V2	cis	Esophagus Mucosa	GTEx
rs10471184	CYP4V2	cis	inferior olivary nucleus	BrainEAC
rs10471184	CYP4V2	cis	intralobular white matter	BrainEAC
rs10471184	CYP4V2	cis	multi-tissue	Pritchard
rs10471184	CYP4V2	cis	parietal	SCAN
rs10471184	CYP4V2	cis	brain	BrainEAC
rs10471184	KLKB1	cis	cerebellum	SCAN

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187113600-187123800	Weak transcription	Fetal Brain Male	brain
2	chr4:187113600-187125200	Weak transcription	Gastric	stomach
3	chr4:187113800-187123200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr4:187113800-187124000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:187113800-187125200	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr4:187113800-187125400	Weak transcription	Esophagus	oesophagus
7	chr4:187113800-187126000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:187113800-187130600	Weak transcription	Stomach Mucosa	stomach
9	chr4:187113800-187131400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:187113800-187132200	Weak transcription	Colonic Mucosa	Colon
11	chr4:187114000-187123000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr4:187114000-187123200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr4:187114000-187124400	Weak transcription	Fetal Lung	lung
14	chr4:187114000-187125200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr4:187114000-187133200	Weak transcription	HSMM	muscle
16	chr4:187114200-187123200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr4:187114200-187123800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr4:187114200-187124200	Weak transcription	K562	blood
19	chr4:187114200-187125200	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr4:187114200-187125200	Weak transcription	NHDF-Ad	bronchial
21	chr4:187114200-187126000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:187114400-187123600	Weak transcription	Fetal Kidney	kidney
23	chr4:187114400-187125200	Weak transcription	Primary hematopoietic stem cells	blood
24	chr4:187114400-187125200	Weak transcription	Osteobl	bone
25	chr4:187114600-187125200	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr4:187114600-187125200	Weak transcription	Right Atrium	heart
27	chr4:187114800-187130000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr4:187115000-187125200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr4:187115000-187125200	Weak transcription	NHLF	lung
30	chr4:187115200-187123800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:187115200-187124400	Weak transcription	Spleen	Spleen
32	chr4:187115200-187125200	Weak transcription	Psoas Muscle	Psoas
33	chr4:187115200-187125600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr4:187115200-187133600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr4:187115400-187123600	Weak transcription	Pancreas	Pancrea
36	chr4:187115400-187125200	Weak transcription	Fetal Brain Female	brain
37	chr4:187115400-187125200	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr4:187115400-187125600	Weak transcription	Brain Substantia Nigra	brain
39	chr4:187115400-187130400	Weak transcription	Small Intestine	intestine
40	chr4:187116800-187123800	Weak transcription	Thymus	Thymus
41	chr4:187116800-187125200	Weak transcription	Brain Angular Gyrus	brain
42	chr4:187116800-187125200	Weak transcription	Right Ventricle	heart
43	chr4:187116800-187125400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr4:187117000-187123000	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr4:187117000-187124800	Weak transcription	Placenta	Placenta
46	chr4:187117200-187125200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr4:187117400-187125600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr4:187117600-187124400	Weak transcription	Lung	lung
49	chr4:187117600-187126200	Weak transcription	Brain Hippocampus Middle	brain
50	chr4:187117600-187140600	Weak transcription	Aorta	Aorta

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