Variant report

Variant	rs6704126
Chromosome Location	chr1:151371305-151371306
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4)
CpG islands
(count:61)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr1:151371240-151371390	GM12873	blood:	n/a	n/a
2	POLR2A	chr1:151371211-151371483	HCT-116	colon:	n/a	n/a
3	GABPA	chr1:151370980-151373412	MCF-7	breast:	n/a	chr1:151372012-151372019
4	MAX	chr1:151371191-151371495	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:151371285-151371335	GM19239	blood:	n/a
2	chr1:151371285-151371335	Caco-2	colon:	n/a
3	chr1:151371285-151371335	A549	lung:	n/a
4	chr1:151371285-151371335	U87	brain:	n/a
5	chr1:151371285-151371335	Hela-S3	cervix:	n/a
6	chr1:151371285-151371335	MCF10A-Er-Src	breast:	n/a
7	chr1:151371285-151371335	SK-N-SH	brain:	n/a
8	chr1:151371285-151371335	NHBE	bronchial:	n/a
9	chr1:151371285-151371335	CMK	blood:	n/a
10	chr1:151371285-151371335	NT2-D1	testis:	n/a
11	chr1:151371285-151371335	H1-hESC	embryonic stem cell:	embryo
12	chr1:151371285-151371335	SKMC	muscle:	n/a
13	chr1:151371285-151371335	Jurkat	blood:	n/a
14	chr1:151371285-151371335	BJ	skin:	n/a
15	chr1:151371285-151371335	PFSK-1	brain:	n/a
16	chr1:151371285-151371335	ProgFib	skin:	n/a
17	chr1:151371285-151371335	ECC-1	luminal epithelium:	n/a
18	chr1:151371285-151371335	HIPEpiC	eye:	n/a
19	chr1:151371285-151371335	HEEpiC	esophagus:	n/a
20	chr1:151371285-151371335	GM12891	blood:	n/a
21	chr1:151371285-151371335	NB4	blood:	n/a
22	chr1:151371285-151371335	HNPCEpiC	eye:	n/a
23	chr1:151371285-151371335	GM12892	blood:	n/a
24	chr1:151371285-151371335	HRCEpiC	kidney:	n/a
25	chr1:151371285-151371335	GM06990	blood:	n/a
26	chr1:151371285-151371335	HepG2	liver:	n/a
27	chr1:151371285-151371335	BE2_C	brain:	n/a
28	chr1:151371285-151371335	T-47D	breast:	n/a
29	chr1:151371285-151371335	GM12878	blood:	n/a
30	chr1:151371285-151371335	HCM	heart:	n/a
31	chr1:151371285-151371335	HUVEC	blood vessel:	n/a
32	chr1:151371285-151371335	AG04450	lung:	fetal
33	chr1:151371285-151371335	PANC-1	pancreas:	n/a
34	chr1:151371285-151371335	IMR90	lung:	fetal
35	chr1:151371285-151371335	Hepatocyte	liver:	n/a
36	chr1:151371285-151371335	HEK293	kidney:	embryo
37	chr1:151371285-151371335	HRE	kidney:	n/a
38	chr1:151371285-151371335	HL-60	blood:	n/a
39	chr1:151371285-151371335	NH-A	brain:	n/a
40	chr1:151371285-151371335	AoSMC	blood vessel:	n/a
41	chr1:151371285-151371335	ovcar-3	ovarian:	n/a
42	chr1:151371285-151371335	MCF-7	breast:	n/a
43	chr1:151371285-151371335	HCF	heart:	n/a
44	chr1:151371285-151371335	NHDF-neo	bronchial:	n/a
45	chr1:151371285-151371335	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:151371285-151371335	SAEC	small airway:	n/a
47	chr1:151371285-151371335	K562	blood:	n/a
48	chr1:151371285-151371335	AG10803	skin:	n/a
49	chr1:151371285-151371335	RPTEC	kidney:	n/a
50	chr1:151371285-151371335	SK-N-MC	brain:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:151368568..151371370-chr1:151392039..151394565,2	K562	blood:
2	chr1:151254429..151257729-chr1:151370560..151375073,7	MCF-7	breast:
3	chr1:151370719..151373828-chr1:151394792..151398021,4	MCF-7	breast:
4	chr1:151341989..151348019-chr1:151370228..151376359,14	MCF-7	breast:
5	chr1:151371183..151372890-chr1:151431011..151433472,2	MCF-7	breast:
6	chr1:151312120..151316742-chr1:151370081..151375586,6	MCF-7	breast:
7	chr1:151318180..151322621-chr1:151370786..151375600,7	K562	blood:
8	chr1:151252692..151257354-chr1:151370358..151373702,7	K562	blood:
9	1:151171193-151178589..1:151368336-151375897	Hela-S3	cervix:
10	chr1:151252566..151256216-chr1:151370228..151373702,9	K562	blood:
11	chr1:151297425..151301136-chr1:151370895..151373723,5	MCF-7	breast:
12	chr1:151370811..151373589-chr1:151512732..151514796,2	K562	blood:
13	1:151368336-151375897..1:151592347-151603110	Hela-S3	cervix:
14	chr1:151273322..151275078-chr1:151370486..151372389,2	MCF-7	breast:
15	chr1:151252229..151256416-chr1:151370480..151373573,6	MCF-7	breast:
16	chr1:151343373..151350462-chr1:151369795..151376328,11	MCF-7	breast:
17	chr1:151317450..151322791-chr1:151370457..151374000,10	MCF-7	breast:
18	chr1:151299305..151301447-chr1:151370337..151372394,3	MCF-7	breast:
19	chr1:151160213..151162825-chr1:151370506..151372060,2	K562	blood:
20	chr1:151319505..151321169-chr1:151370320..151372349,2	MCF-7	breast:
21	chr1:151162193..151163907-chr1:151370731..151372764,2	MCF-7	breast:
22	chr1:151344758..151345571-chr1:151371234..151372258,3	MCF-7	breast:

No data

Variant related genes	Relation type
PSMB4	TF binding region
PSMB4	CpG island
ENSG00000237976	Chromatin interaction
ENSG00000206635	Chromatin interaction
ENSG00000143390	Chromatin interaction
ENSG00000232671	Chromatin interaction
ENSG00000273481	Chromatin interaction
ENSG00000143373	Chromatin interaction
ENSG00000143442	Chromatin interaction
ENSG00000143416	Chromatin interaction
ENSG00000232536	Chromatin interaction
ENSG00000265753	Chromatin interaction
ENSG00000224645	Chromatin interaction
ENSG00000163159	Chromatin interaction
ENSG00000143367	Chromatin interaction
ENSG00000143398	Chromatin interaction
ENSG00000143393	Chromatin interaction

Extended variants
information (count: 69 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11204806	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11204820	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12566457	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12566673	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1539493	1.00[CEU][hapmap];0.91[CHB][hapmap];0.87[GIH][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap]
rs1571294	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16833248	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16833263	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16833274	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2296840	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3748549	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3818561	1.00[CEU][hapmap]
rs4147451	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4354539	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4970953	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4971045	0.82[EUR][1000 genomes]
rs56317453	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58057716	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59153459	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59848815	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6587574	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6587586	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6669679	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67750241	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72633634	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72633635	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72633636	0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs72633637	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72633638	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72633639	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7548614	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9729256	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:37 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916272	chr1:150961809-151557253	Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	219 gene(s)	inside rSNPs	diseases
2	esv34461	chr1:151240542-151411635	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
3	esv2753774	chr1:151240542-151411635	Genic enhancers Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
4	nsv831581	chr1:151289151-151478605	Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
5	nsv872424	chr1:151325055-151413180	Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
6	nsv872425	chr1:151325055-151413790	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	esv2756864	chr1:151328794-151411635	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
8	esv2758969	chr1:151328794-151411635	Flanking Active TSS Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv872427	chr1:151329138-151371305	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	23 gene(s)	inside rSNPs	diseases
10	nsv872428	chr1:151329138-151395782	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	32 gene(s)	inside rSNPs	diseases
11	nsv872429	chr1:151329138-151413180	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
12	nsv8380	chr1:151329887-151410346	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
13	esv2753659	chr1:151330927-151384927	Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	32 gene(s)	inside rSNPs	diseases
14	nsv824575	chr1:151331533-151408096	Enhancers Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
15	nsv463761	chr1:151333167-151404848	Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
16	nsv463772	chr1:151333167-151404848	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
17	nsv463783	chr1:151333167-151404848	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
18	nsv463794	chr1:151333167-151404848	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
19	nsv463805	chr1:151333167-151404848	ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
20	nsv463816	chr1:151333167-151404848	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
21	nsv470737	chr1:151333167-151404848	Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
22	nsv547849	chr1:151333167-151404848	Strong transcription Transcr. at gene 5' and 3' Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
23	nsv818467	chr1:151333167-151404848	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
24	nsv463827	chr1:151333167-151413180	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
25	nsv547850	chr1:151333167-151413180	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
26	nsv1011398	chr1:151333430-151402839	Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
27	nsv872430	chr1:151334796-151413180	Strong transcription Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
28	nsv441714	chr1:151336699-151397878	Strong transcription Genic enhancers Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	32 gene(s)	inside rSNPs	diseases
29	esv2753719	chr1:151337788-151373200	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
30	nsv463839	chr1:151338570-151404848	Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
31	nsv547851	chr1:151338570-151404848	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
32	nsv872431	chr1:151338570-151413180	Strong transcription Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
33	nsv872432	chr1:151339196-151413180	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
34	nsv872433	chr1:151341417-151413180	Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	32 gene(s)	inside rSNPs	diseases
35	nsv872434	chr1:151347820-151413180	Genic enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	32 gene(s)	inside rSNPs	diseases
36	nsv872435	chr1:151351060-151413180	Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	32 gene(s)	inside rSNPs	diseases
37	nsv872436	chr1:151357333-151413180	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	32 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6704126	PSMB4	cis	lymphoblastoid	seeQTL

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151370800-151371400	Enhancers	Primary B cells from peripheral blood	blood
2	chr1:151370800-151371400	Weak transcription	Fetal Kidney	kidney
3	chr1:151370800-151371400	Weak transcription	HepG2	liver
4	chr1:151371000-151371400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr1:151371000-151371400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr1:151371200-151371400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
7	chr1:151371200-151371400	Enhancers	Primary T cells from cord blood	blood
8	chr1:151371200-151371400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
9	chr1:151371200-151371400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr1:151371200-151371400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr1:151371200-151371400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
12	chr1:151371200-151371400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr1:151371200-151371400	Enhancers	Brain Hippocampus Middle	brain
14	chr1:151371200-151371400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr1:151371200-151371400	Enhancers	Fetal Muscle Leg	muscle
16	chr1:151371200-151371400	Enhancers	Placenta	Placenta
17	chr1:151371200-151371400	Enhancers	Fetal Thymus	thymus
18	chr1:151371200-151371400	Enhancers	Thymus	Thymus
19	chr1:151371200-151371400	Flanking Active TSS	A549	lung
20	chr1:151371200-151371400	Active TSS	Monocytes-CD14+_RO01746	blood
21	chr1:151371200-151371600	Enhancers	Primary B cells from cord blood	blood
22	chr1:151371200-151371600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
23	chr1:151371200-151371600	Enhancers	Fetal Stomach	stomach
24	chr1:151371200-151371600	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr1:151371200-151371600	Flanking Active TSS	Dnd41	blood
26	chr1:151371200-151371600	Enhancers	NHLF	lung
27	chr1:151371200-151372000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:151371200-151372200	Active TSS	Primary T helper cells fromperipheralblood	blood
29	chr1:151371200-151372200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr1:151371200-151372200	Active TSS	Rectal Smooth Muscle	rectum
31	chr1:151371200-151372400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
32	chr1:151371200-151372600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:151371200-151372800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr1:151371200-151372800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr1:151371200-151372800	Active TSS	Fetal Brain Female	brain
36	chr1:151371200-151372800	Active TSS	NHEK	skin
37	chr1:151371200-151372800	Active TSS	Osteobl	bone
38	chr1:151371200-151373000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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