Variant report

Variant	rs4074838
Chromosome Location	chr7:100032665-100032666
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:93)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:93 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr7:100032223-100033760	GM12891	blood:	n/a	n/a
2	POLR2A	chr7:100032140-100034606	GM12892	blood:	n/a	n/a
3	POLR2A	chr7:100032543-100034503	HCT-116	colon:	n/a	n/a
4	POLR2A	chr7:100032407-100034492	PBDE	blood:	n/a	n/a
5	POLR2A	chr7:100032282-100034553	GM12878	blood:	n/a	n/a
6	HEY1	chr7:100032290-100032779	K562	blood:	n/a	chr7:100032696-100032705
7	POLR2A	chr7:100032311-100034491	K562	blood:	n/a	n/a
8	POLR2A	chr7:100032169-100034606	GM12891	blood:	n/a	n/a
9	POLR2A	chr7:100032545-100034560	ECC-1	luminal epithelium:	n/a	n/a
10	POLR2A	chr7:100032497-100034528	GM18505	blood:	n/a	n/a
11	POLR2A	chr7:100032219-100034537	MCF10A-Er-Src	breast:	n/a	n/a
12	POLR2A	chr7:100032217-100034542	HL-60	blood:	n/a	n/a
13	POLR2A	chr7:100032284-100034495	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr7:100030180-100034516	HepG2	liver:	n/a	n/a
15	POLR2A	chr7:100032436-100032857	SK-N-SH	brain:	n/a	n/a
16	HCFC1	chr7:100032210-100034610	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr7:100032653-100032674	ProgFib	skin:	n/a	n/a
18	PML	chr7:100032441-100033720	K562	blood:	n/a	n/a
19	POLR2A	chr7:100032179-100032799	GM12878	blood:	n/a	n/a
20	POLR2A	chr7:100032227-100032826	GM12878	blood:	n/a	n/a
21	POLR2A	chr7:100032212-100034595	HL-60	blood:	n/a	n/a
22	MTA3	chr7:100030193-100034606	GM12878	blood:	n/a	n/a
23	POLR2A	chr7:100032362-100034534	NB4	blood:	n/a	n/a
24	POLR2A	chr7:100032302-100034495	K562	blood:	n/a	n/a
25	NR2F2	chr7:100032416-100033746	K562	blood:	n/a	n/a
26	POLR2A	chr7:100032245-100033680	GM12891	blood:	n/a	n/a
27	CBX3	chr7:100032265-100032821	K562	blood:	n/a	n/a
28	POLR2A	chr7:100032311-100034448	K562	blood:	n/a	n/a
29	POLR2A	chr7:100029646-100033719	U87	brain:	n/a	n/a
30	POLR2A	chr7:100032291-100034505	GM12878	blood:	n/a	n/a
31	POLR2A	chr7:100032609-100032756	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr7:100025552-100034611	GM12892	blood:	n/a	n/a
33	POLR2A	chr7:100025685-100034590	GM12892	blood:	n/a	n/a
34	POLR2A	chr7:100025716-100034505	K562	blood:	n/a	n/a
35	POLR2A	chr7:100032246-100034604	MCF-7	breast:	n/a	n/a
36	POLR2A	chr7:100032230-100034480	U87	brain:	n/a	n/a
37	POLR2A	chr7:100025714-100034420	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr7:100032202-100034560	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr7:100025516-100034612	SK-N-MC	brain:	n/a	n/a
40	TAL1	chr7:100032449-100032752	K562	blood:	n/a	n/a
41	POLR2A	chr7:100032161-100033691	SK-N-MC	brain:	n/a	n/a
42	NR2F2	chr7:100032346-100032905	K562	blood:	n/a	n/a
43	POLR2A	chr7:100025670-100034884	K562	blood:	n/a	n/a
44	POLR2A	chr7:100032163-100034571	K562	blood:	n/a	n/a
45	PBX3	chr7:100032442-100034557	SK-N-SH	brain:	n/a	n/a
46	TEAD4	chr7:100032277-100033750	K562	blood:	n/a	n/a
47	STAT5A	chr7:100032354-100034587	GM12878	blood:	n/a	chr7:100033901-100033925
48	POLR2A	chr7:100032170-100034619	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr7:100032332-100034560	HUVEC	blood vessel:	n/a	n/a
50	SIX5	chr7:100032453-100033232	A549	lung:	n/a	n/a

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100032492..100035080-chr7:100065519..100068625,3	MCF-7	breast:
2	chr7:99998986..100001461-chr7:100032501..100034124,2	K562	blood:
3	chr7:100031120..100032907-chr7:100059800..100061803,2	K562	blood:
4	chr7:100025583..100035841-chr7:100071553..100080023,19	MCF-7	breast:
5	chr7:99677604..99679757-chr7:100032184..100034035,2	K562	blood:
6	chr7:99997930..100000096-chr7:100032489..100035082,2	MCF-7	breast:
7	chr7:100031790..100034595-chr7:100181557..100184454,2	MCF-7	breast:
8	chr7:100031924..100034212-chr7:100179842..100183716,3	MCF-7	breast:
9	chr7:100032100..100034084-chr7:100269925..100271746,2	MCF-7	breast:
10	chr19:12903211..12903980-chr7:100032571..100033277,2	Hela-S3	cervix:
11	chr7:100018468..100021635-chr7:100028917..100032766,4	K562	blood:
12	chr7:99691882..99693394-chr7:100030103..100032798,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000240211	TF binding region
ENSG00000241357	TF binding region
ENSG00000172354	Chromatin interaction
ENSG00000166526	Chromatin interaction
ENSG00000166925	Chromatin interaction
ENSG00000264758	Chromatin interaction
ENSG00000166508	Chromatin interaction
ENSG00000095066	Chromatin interaction
ENSG00000077454	Chromatin interaction
ENSG00000106336	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000185955	Chromatin interaction

Extended variants
information (count: 98 )
Associated
traits (count: 57 )

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs1000215	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10085549	0.83[CHD][hapmap];1.00[GIH][hapmap]
rs10241492	0.93[CEU][hapmap];0.93[YRI][hapmap]
rs1073	1.00[ASW][hapmap];0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][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]
rs11559117	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];1.00[ASN][1000 genomes]
rs11760536	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap]
rs11761253	0.87[ASW][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap]
rs11761624	1.00[ASN][1000 genomes]
rs11761725	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11761784	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11763414	0.93[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11763511	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[ASN][1000 genomes]
rs11764818	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11765869	0.83[CHD][hapmap];1.00[GIH][hapmap]
rs11766202	1.00[ASN][1000 genomes]
rs11766752	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11769057	0.87[ASW][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.93[MKK][hapmap]
rs11769700	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];1.00[ASN][1000 genomes]
rs11769886	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11771241	0.93[CEU][hapmap];0.93[YRI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11771419	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs11772580	1.00[ASN][1000 genomes]
rs11773661	0.93[CEU][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1962269	0.85[CEU][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2003507	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2406253	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];1.00[ASN][1000 genomes]
rs2406255	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28490152	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28578163	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28629346	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28660238	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2897358	1.00[ASN][1000 genomes]
rs34989573	0.86[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];1.00[ASN][1000 genomes]
rs35111986	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3900792	1.00[ASW][hapmap];0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.88[LWK][hapmap];0.85[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4385401	1.00[ASN][1000 genomes]
rs4463351	1.00[ASN][1000 genomes]
rs4469386	1.00[ASN][1000 genomes]
rs4472444	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4989959	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60257855	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60478351	1.00[ASN][1000 genomes]
rs60644673	1.00[ASN][1000 genomes]
rs60844404	1.00[ASN][1000 genomes]
rs66632384	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs66648318	1.00[ASN][1000 genomes]
rs66958101	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67040465	0.86[ASN][1000 genomes]
rs67163493	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67196635	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67239991	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67315960	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67471932	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67483801	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67885733	1.00[ASN][1000 genomes]
rs68116612	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6945952	1.00[ASW][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.88[LWK][hapmap];0.93[MKK][hapmap];0.93[YRI][hapmap]
rs6946768	1.00[GIH][hapmap]
rs6948685	0.87[ASW][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.93[MKK][hapmap]
rs6948699	1.00[ASN][1000 genomes]
rs6953107	1.00[ASN][1000 genomes]
rs6953749	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6955362	0.88[ASW][hapmap];0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.94[LWK][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6955367	0.83[CHD][hapmap];1.00[GIH][hapmap]
rs6957928	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6962151	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6965458	0.83[CHD][hapmap];1.00[GIH][hapmap]
rs6970806	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6970828	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6972167	0.86[ASN][1000 genomes]
rs6974286	1.00[ASN][1000 genomes]
rs6975514	0.93[CEU][hapmap];1.00[YRI][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6975729	1.00[ASW][hapmap];0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][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]
rs6978739	1.00[ASN][1000 genomes]
rs6979335	1.00[ASN][1000 genomes]
rs705866	0.83[CHD][hapmap];1.00[GIH][hapmap]
rs73161759	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73161762	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73403312	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73405353	1.00[ASN][1000 genomes]
rs7783159	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7783550	1.00[ASW][hapmap];0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.85[EUR][1000 genomes]
rs7787620	0.85[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];1.00[ASN][1000 genomes]
rs7787825	1.00[ASN][1000 genomes]
rs7794485	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7800667	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7803454	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7809801	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7811142	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3350965	chr7:99747460-100146105	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
2	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
3	nsv831071	chr7:99918025-100113413	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	287 gene(s)	inside rSNPs	diseases
4	nsv527107	chr7:100014711-100064719	Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	269 gene(s)	inside rSNPs	diseases
5	nsv888776	chr7:100014711-100198386	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	297 gene(s)	inside rSNPs	diseases
6	nsv888777	chr7:100014711-100221867	Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
7	nsv888778	chr7:100014711-100236593	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	310 gene(s)	inside rSNPs	diseases
8	nsv888779	chr7:100014711-100313420	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	321 gene(s)	inside rSNPs	diseases
9	nsv888780	chr7:100032665-100198386	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases

mRNA abundance (count:57)

SNP	Gene	Cis/trans	Tissue	Source
rs4074838	PILRB	cis	Artery Tibial	GTEx
rs4074838	PILRA	cis	Heart Left Ventricle	GTEx
rs4074838	TRIM4	Cis_1M	lymphoblastoid	RTeQTL
rs4074838	PILRB	cis	Thyroid	GTEx
rs4074838	PILRB	cis	cerebellum	SCAN
rs4074838	PILRB	cis	Artery Aorta	GTEx
rs4074838	PVRIG2P	cis	Artery Tibial	GTEx
rs4074838	MEPCE	cis	lymphoblastoid	seeQTL
rs4074838	CNPY4	cis	cerebellum	SCAN
rs4074838	PVRIG2P	cis	Thyroid	GTEx
rs4074838	PVRIG2P	cis	Nerve Tibial	GTEx
rs4074838	STAG3L5P	cis	Artery Tibial	GTEx
rs4074838	PILRB	cis	Esophagus Muscularis	GTEx
rs4074838	PILRB	cis	Adipose Subcutaneous	GTEx
rs4074838	PVRIG2P	cis	Adipose Subcutaneous	GTEx
rs4074838	GNB2	cis	parietal	SCAN
rs4074838	PILRA	cis	Muscle Skeletal	GTEx
rs4074838	PILRB	cis	Whole Blood	GTEx
rs4074838	PILRA	cis	Stomach	GTEx
rs4074838	PILRB	cis	multi-tissue	Pritchard
rs4074838	GATS	cis	parietal	SCAN
rs4074838	STAG3L5P	cis	Esophagus Muscularis	GTEx
rs4074838	STAG3L5P	cis	Skin Sun Exposed Lower leg	GTEx
rs4074838	PILRA	cis	Artery Aorta	GTEx
rs4074838	ZCWPW1	cis	cerebellum	SCAN
rs4074838	PILRB	cis	Esophagus Mucosa	GTEx
rs4074838	PILRA	cis	Esophagus Muscularis	GTEx
rs4074838	PILRA	cis	Esophagus Mucosa	GTEx
rs4074838	PILRB	Cis_1M	lymphoblastoid	RTeQTL
rs4074838	ZCWPW1	cis	parietal	SCAN
rs4074838	PVRIG2P	cis	lung	GTEx
rs4074838	PILRA	cis	cerebellum	SCAN
rs4074838	PILRB	cis	Skin Sun Exposed Lower leg	GTEx
rs4074838	PMS2P1	cis	Thyroid	GTEx
rs4074838	PILRA	cis	Artery Tibial	GTEx
rs4074838	PILRB	cis	Nerve Tibial	GTEx
rs4074838	STAG3L5P	cis	Thyroid	GTEx
rs4074838	PILRB	cis	parietal	SCAN
rs4074838	PILRA	cis	Adipose Subcutaneous	GTEx
rs4074838	STAG3L5P	cis	Nerve Tibial	GTEx
rs4074838	STAG3L5P	cis	lung	GTEx
rs4074838	STAG3L5P	cis	Heart Left Ventricle	GTEx
rs4074838	PILRA	cis	Nerve Tibial	GTEx
rs4074838	PILRA	cis	Skin Sun Exposed Lower leg	GTEx
rs4074838	PILRA	cis	parietal	SCAN
rs4074838	PILRB	cis	Muscle Skeletal	GTEx
rs4074838	PILRB	cis	Heart Left Ventricle	GTEx
rs4074838	PILRA	cis	Thyroid	GTEx
rs4074838	PILRB	cis	lung	GTEx
rs4074838	PILRB	cis	lymphoblastoid	seeQTL
rs4074838	STAG3L5P	cis	Esophagus Mucosa	GTEx
rs4074838	PVRIG2P	cis	Esophagus Mucosa	GTEx
rs4074838	PVRIG	Cis_1M	lymphoblastoid	RTeQTL
rs4074838	PVRIG	cis	cerebellum	SCAN
rs4074838	STAG3L5P	cis	Muscle Skeletal	GTEx
rs4074838	STAG3L5P	cis	Adipose Subcutaneous	GTEx
rs4074838	STAG3L5P	cis	Artery Aorta	GTEx

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100027400-100033600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr7:100028200-100033400	Transcr. at gene 5' and 3'	Dnd41	blood
3	chr7:100028600-100033600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr7:100028800-100033000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:100028800-100033000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr7:100028800-100033000	Genic enhancers	Placenta	Placenta
7	chr7:100028800-100033000	Genic enhancers	Spleen	Spleen
8	chr7:100029000-100033000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
9	chr7:100029400-100033000	Transcr. at gene 5' and 3'	Hela-S3	cervix
10	chr7:100030400-100032800	Strong transcription	Brain Cingulate Gyrus	brain
11	chr7:100031400-100032800	Genic enhancers	Colonic Mucosa	Colon
12	chr7:100031600-100032800	Genic enhancers	Pancreas	Pancrea
13	chr7:100031600-100033000	Genic enhancers	Primary B cells from peripheral blood	blood
14	chr7:100031600-100033000	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
15	chr7:100031800-100033000	Weak transcription	Aorta	Aorta
16	chr7:100031800-100033000	Weak transcription	Ovary	ovary
17	chr7:100032000-100032800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr7:100032000-100033000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:100032000-100033000	Enhancers	Placenta Amnion	Placenta Amnion
20	chr7:100032200-100032800	Transcr. at gene 5' and 3'	HUES48 Cell Line	embryonic stem cell
21	chr7:100032200-100032800	Transcr. at gene 5' and 3'	Primary B cells from cord blood	blood
22	chr7:100032200-100032800	Genic enhancers	Brain Inferior Temporal Lobe	brain
23	chr7:100032200-100032800	Genic enhancers	Sigmoid Colon	Sigmoid Colon
24	chr7:100032200-100033000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
25	chr7:100032200-100033000	Enhancers	Stomach Mucosa	stomach
26	chr7:100032200-100033200	Transcr. at gene 5' and 3'	K562	blood
27	chr7:100032200-100033600	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:100032200-100034600	Active TSS	Psoas Muscle	Psoas
29	chr7:100032400-100032800	Transcr. at gene 5' and 3'	H1 Cell Line	embryonic stem cell
30	chr7:100032400-100032800	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
31	chr7:100032400-100032800	Transcr. at gene 5' and 3'	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr7:100032400-100032800	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
33	chr7:100032400-100032800	Genic enhancers	Primary monocytes fromperipheralblood	blood
34	chr7:100032400-100032800	Transcr. at gene 5' and 3'	Primary T helper cells fromperipheralblood	blood
35	chr7:100032400-100032800	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr7:100032400-100032800	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr7:100032400-100032800	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:100032400-100032800	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
39	chr7:100032400-100032800	Genic enhancers	Brain Hippocampus Middle	brain
40	chr7:100032400-100032800	Transcr. at gene 5' and 3'	Colon Smooth Muscle	Colon
41	chr7:100032400-100032800	Transcr. at gene 5' and 3'	Duodenum Smooth Muscle	Duodenum
42	chr7:100032400-100032800	Transcr. at gene 5' and 3'	HMEC	breast
43	chr7:100032400-100032800	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
44	chr7:100032400-100032800	Transcr. at gene 5' and 3'	NH-A	brain
45	chr7:100032400-100032800	Transcr. at gene 5' and 3'	NHDF-Ad	bronchial
46	chr7:100032400-100033000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:100032400-100033000	Transcr. at gene 5' and 3'	iPS-15b Cell Line	embryonic stem cell
48	chr7:100032400-100033000	Transcr. at gene 5' and 3'	iPS-18 Cell Line	embryonic stem cell
49	chr7:100032400-100033000	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
50	chr7:100032400-100033000	Transcr. at gene 5' and 3'	Ganglion Eminence derived primary cultured neurospheres	brain

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